Linked Data
ClinVar Variation Id:
142960
ClinVar RCV Id:
RCV000132452
RCV000214828
RCV000226690
RCV000411483
RCV000656944
RCV000708988
RCV003390826
dbSNP Id:
rs587782852
ExAC:
7:6031609 T / C
gnomAD v2:
7-6031609-T-C
gnomAD v3:
7-5991978-T-C
gnomAD v4:
7-5991978-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.5991978T>C , CM000669.2:g.5991978T>C | GRCh38 |
| NC_000007.13:g.6031609T>C , CM000669.1:g.6031609T>C | GRCh37 |
| NC_000007.12:g.5998135T>C | NCBI36 |
| NG_008466.1:g.22129A>G , LRG_161:g.22129A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699814.2:c.*379A>G | ENSP00000514615.2:n.*379A>G | |
| ENST00000699840.2:c.980A>G | ENSP00000514638.2:p.Asp327Gly | |
| ENST00000699930.2:c.875A>G | ENSP00000514695.2:p.Asp292Gly | |
| ENST00000406569.8:c.983A>G | ENSP00000514464.1:p.Asp328Gly | |
| ENST00000644110.2:c.*577A>G | ENSP00000496392.2:n.*577A>G | |
| ENST00000699752.1:c.983A>G | ENSP00000514561.1:p.Asp328Gly | |
| ENST00000699753.1:c.*282A>G | ENSP00000514562.1:n.*282A>G | |
| ENST00000699754.1:c.785A>G | ENSP00000514563.1:p.Asp262Gly | |
| ENST00000699755.1:c.*382A>G | ENSP00000514564.1:n.*382A>G | |
| ENST00000699756.1:c.*570A>G | ENSP00000514565.1:n.*570A>G | |
| ENST00000699757.1:c.*240A>G | ENSP00000514566.1:n.*240A>G | |
| ENST00000699758.1:c.*240A>G | ENSP00000514567.1:n.*240A>G | |
| ENST00000699759.1:n.1837A>G | ||
| ENST00000699760.1:c.665A>G | ENSP00000514568.1:p.Asp222Gly | |
| ENST00000699761.1:c.578A>G | ENSP00000514569.1:p.Asp193Gly | |
| ENST00000699762.1:c.410A>G | ENSP00000514570.1:p.Asp137Gly | |
| ENST00000699763.1:c.578A>G | ENSP00000514571.1:p.Asp193Gly | |
| ENST00000699764.1:c.983A>G | ENSP00000514572.1:p.Asp328Gly | |
| ENST00000699765.1:c.*79A>G | ENSP00000514573.1:n.*79A>G | |
| ENST00000699766.1:c.983A>G | ENSP00000514574.1:p.Asp328Gly | |
| ENST00000699767.1:c.983A>G | ENSP00000514575.1:p.Asp328Gly | |
| ENST00000699768.1:c.983A>G | ENSP00000514576.1:p.Asp328Gly | |
| ENST00000699811.1:c.578A>G | ENSP00000514614.1:p.Asp193Gly | |
| ENST00000699813.1:n.1096A>G | ||
| ENST00000699814.1:c.606A>G | ||
| ENST00000699815.1:c.*475A>G | ENSP00000514616.1:n.*475A>G | |
| ENST00000699816.1:c.578A>G | ENSP00000514617.1:p.Asp193Gly | |
| ENST00000699817.1:c.*577A>G | ENSP00000514618.1:n.*577A>G | |
| ENST00000699818.1:c.578A>G | ENSP00000514619.1:p.Asp193Gly | |
| ENST00000699819.1:c.*140A>G | ENSP00000514620.1:n.*140A>G | |
| ENST00000699820.1:c.983A>G | ENSP00000514621.1:p.Asp328Gly | |
| ENST00000699821.1:c.578A>G | ENSP00000514622.1:p.Asp193Gly | |
| ENST00000699822.1:c.*435A>G | ENSP00000514623.1:n.*435A>G | |
| ENST00000699823.1:c.578A>G | ENSP00000514624.1:p.Asp193Gly | |
| ENST00000699824.1:c.*486A>G | ENSP00000514625.1:n.*486A>G | |
| ENST00000699825.1:c.578A>G | ENSP00000514626.1:p.Asp193Gly | |
| ENST00000699826.1:c.*382A>G | ENSP00000514627.1:n.*382A>G | |
| ENST00000699827.1:c.815A>G | ENSP00000514628.1:p.Asp272Gly | |
| ENST00000699828.1:c.983A>G | ENSP00000514629.1:p.Asp328Gly | |
| ENST00000699829.1:c.*484A>G | ENSP00000514630.1:n.*484A>G | |
| ENST00000699830.1:c.*382A>G | ENSP00000514631.1:n.*382A>G | |
| ENST00000699833.1:n.2755A>G | ||
| ENST00000699837.1:c.578A>G | ENSP00000514635.1:p.Asp193Gly | |
| ENST00000699838.1:c.*883A>G | ENSP00000514636.1:n.*883A>G | |
| ENST00000699839.1:c.1169A>G | ENSP00000514637.1:p.Asp390Gly | |
| ENST00000699840.1:c.980A>G | ENSP00000514638.1:p.Asp327Gly | |
| ENST00000699916.1:c.*240A>G | ENSP00000514684.1:n.*240A>G | |
| ENST00000699917.1:c.*432A>G | ENSP00000514685.1:n.*432A>G | |
| ENST00000699918.1:c.*484A>G | ENSP00000514686.1:n.*484A>G | |
| ENST00000699919.1:c.*570A>G | ENSP00000514687.1:n.*570A>G | |
| ENST00000699920.1:c.*619A>G | ENSP00000514688.1:n.*619A>G | |
| ENST00000699928.1:c.983A>G | ENSP00000514693.1:p.Asp328Gly | |
| ENST00000699929.1:c.*284A>G | ENSP00000514694.1:n.*284A>G | |
| ENST00000699930.1:c.875A>G | ENSP00000514695.1:p.Asp292Gly | |
| ENST00000699931.1:n.2411A>G | ||
| ENST00000699932.1:c.*79A>G | ENSP00000514696.1:n.*79A>G | |
| ENST00000699933.1:n.963A>G | ||
| ENST00000699951.1:c.*79A>G | ENSP00000514706.1:n.*79A>G | |
| ENST00000699952.1:c.803+5348A>G | ENSP00000514707.1:n.803+5348A>G | |
| ENST00000699953.1:c.*90A>G | ENSP00000514708.1:n.*90A>G | |
| ENST00000699954.1:c.*284A>G | ENSP00000514709.1:n.*284A>G | |
| ENST00000265849.12:c.983A>G MANE Select | ENSP00000265849.7:p.Asp328Gly | |
| ENST00000642292.1:c.578A>G | ENSP00000495524.1:p.Asp193Gly | |
| ENST00000642456.1:c.578A>G | ENSP00000493814.1:p.Asp193Gly | |
| ENST00000643595.1:c.*382A>G | ENSP00000494497.1:n.*382A>G | |
| ENST00000644110.1:c.665A>G | ENSP00000496392.1:p.Asp222Gly | |
| ENST00000265849.11:c.983A>G | ENSP00000265849.7:p.Asp328Gly | |
| ENST00000382321.5:c.803+5348A>G | ENSP00000371758.4:n.803+5348A>G | |
| ENST00000406569.7:n.983A>G | ||
| ENST00000441476.6:c.665A>G | ENSP00000392843.2:p.Asp222Gly | |
| ENST00000469652.1:n.63-9073A>G | ||
| NM_000535.5:c.983A>G , LRG_161t1:c.983A>G | NP_000526.1:p.Asp328Gly | |
| NR_003085.2:n.1065A>G | ||
| XM_006715742.2:c.977A>G | XP_006715805.1:p.Asp326Gly | |
| XM_006715744.2:c.50A>G | XP_006715807.1:p.Asp17Gly | |
| XM_011515427.1:c.1028A>G | XP_011513729.1:p.Asp343Gly | |
| XM_011515428.1:c.1028A>G | XP_011513730.1:p.Asp343Gly | |
| XM_011515429.1:c.665A>G | XP_011513731.1:p.Asp222Gly | |
| XM_011515430.1:c.665A>G | XP_011513732.1:p.Asp222Gly | |
| NM_000535.6:c.983A>G | NP_000526.2:p.Asp328Gly | |
| NM_001322003.1:c.578A>G | NP_001308932.1:p.Asp193Gly | |
| NM_001322004.1:c.578A>G | NP_001308933.1:p.Asp193Gly | |
| NM_001322005.1:c.578A>G | NP_001308934.1:p.Asp193Gly | |
| NM_001322006.1:c.983A>G | NP_001308935.1:p.Asp328Gly | |
| NM_001322007.1:c.665A>G | NP_001308936.1:p.Asp222Gly | |
| NM_001322008.1:c.665A>G | NP_001308937.1:p.Asp222Gly | |
| NM_001322009.1:c.578A>G | NP_001308938.1:p.Asp193Gly | |
| NM_001322010.1:c.578A>G | NP_001308939.1:p.Asp193Gly | |
| NM_001322011.1:c.50A>G | NP_001308940.1:p.Asp17Gly | |
| NM_001322012.1:c.50A>G | NP_001308941.1:p.Asp17Gly | |
| NM_001322013.1:c.410A>G | NP_001308942.1:p.Asp137Gly | |
| NM_001322014.1:c.983A>G | NP_001308943.1:p.Asp328Gly | |
| NM_001322015.1:c.674A>G | NP_001308944.1:p.Asp225Gly | |
| NR_136154.1:n.1070A>G | ||
| XM_006715744.4:c.50A>G | XP_006715807.1:p.Asp17Gly | |
| XM_017012342.2:c.50A>G | XP_016867831.1:p.Asp17Gly | |
| XM_024446800.1:c.578A>G | XP_024302568.1:p.Asp193Gly | |
| NM_000535.7:c.983A>G MANE Select | NP_000526.2:p.Asp328Gly | |
| NM_001322003.2:c.578A>G | NP_001308932.1:p.Asp193Gly | |
| NM_001322004.2:c.578A>G | NP_001308933.1:p.Asp193Gly | |
| NM_001322005.2:c.578A>G | NP_001308934.1:p.Asp193Gly | |
| NM_001322006.2:c.983A>G | NP_001308935.1:p.Asp328Gly | |
| NM_001322008.2:c.665A>G | NP_001308937.1:p.Asp222Gly | |
| NM_001322009.2:c.578A>G | NP_001308938.1:p.Asp193Gly | |
| NM_001322010.2:c.578A>G | NP_001308939.1:p.Asp193Gly | |
| NM_001322011.2:c.50A>G | NP_001308940.1:p.Asp17Gly | |
| NM_001322012.2:c.50A>G | NP_001308941.1:p.Asp17Gly | |
| NM_001322013.2:c.410A>G | NP_001308942.1:p.Asp137Gly | |
| NM_001322014.2:c.983A>G | NP_001308943.1:p.Asp328Gly | |
| NM_001322015.2:c.674A>G | NP_001308944.1:p.Asp225Gly | |
| NM_001322007.2:c.665A>G | NP_001308936.1:p.Asp222Gly |