Linked Data
ClinVar Variation Id:
525606
dbSNP Id:
rs1179605136
gnomAD v3:
7-5986910-C-A
gnomAD v4:
7-5986910-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.5986910C>A , CM000669.2:g.5986910C>A | GRCh38 |
| NC_000007.13:g.6026541C>A , CM000669.1:g.6026541C>A | GRCh37 |
| NC_000007.12:g.5993067C>A | NCBI36 |
| NG_008466.1:g.27197G>T , LRG_161:g.27197G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699814.2:c.*1251G>T | ENSP00000514615.2:n.*1251G>T | |
| ENST00000699840.2:c.1852G>T | ENSP00000514638.2:p.Asp618Tyr | |
| ENST00000699930.2:c.1747G>T | ENSP00000514695.2:p.Asp583Tyr | |
| ENST00000406569.8:c.1678+177G>T | ENSP00000514464.1:n.1678+177G>T | |
| ENST00000644110.2:c.*1449G>T | ENSP00000496392.2:n.*1449G>T | |
| ENST00000699752.1:c.1699G>T | ENSP00000514561.1:p.Asp567Tyr | |
| ENST00000699753.1:c.*1276G>T | ENSP00000514562.1:n.*1276G>T | |
| ENST00000699754.1:c.1657G>T | ENSP00000514563.1:p.Asp553Tyr | |
| ENST00000699755.1:c.*1254G>T | ENSP00000514564.1:n.*1254G>T | |
| ENST00000699756.1:c.*1442G>T | ENSP00000514565.1:n.*1442G>T | |
| ENST00000699757.1:c.*1112G>T | ENSP00000514566.1:n.*1112G>T | |
| ENST00000699758.1:c.*1112G>T | ENSP00000514567.1:n.*1112G>T | |
| ENST00000699759.1:n.2709G>T | ||
| ENST00000699760.1:c.1537G>T | ENSP00000514568.1:p.Asp513Tyr | |
| ENST00000699761.1:c.1450G>T | ENSP00000514569.1:p.Asp484Tyr | |
| ENST00000699762.1:c.1282G>T | ENSP00000514570.1:p.Asp428Tyr | |
| ENST00000699763.1:c.*945G>T | ENSP00000514571.1:n.*945G>T | |
| ENST00000699764.1:c.*173G>T | ENSP00000514572.1:n.*173G>T | |
| ENST00000699765.1:c.*951G>T | ENSP00000514573.1:n.*951G>T | |
| ENST00000699766.1:c.1855G>T | ENSP00000514574.1:p.Asp619Tyr | |
| ENST00000699767.1:c.1855G>T | ENSP00000514575.1:p.Asp619Tyr | |
| ENST00000699768.1:c.1855G>T | ENSP00000514576.1:p.Asp619Tyr | |
| ENST00000699811.1:c.1450G>T | ENSP00000514614.1:p.Asp484Tyr | |
| ENST00000699813.1:n.1968G>T | ||
| ENST00000699814.1:c.1478G>T | ||
| ENST00000699815.1:c.*1386G>T | ENSP00000514616.1:n.*1386G>T | |
| ENST00000699816.1:c.*745G>T | ENSP00000514617.1:n.*745G>T | |
| ENST00000699817.1:c.*1449G>T | ENSP00000514618.1:n.*1449G>T | |
| ENST00000699818.1:c.1450G>T | ENSP00000514619.1:p.Asp484Tyr | |
| ENST00000699819.1:c.*1012G>T | ENSP00000514620.1:n.*1012G>T | |
| ENST00000699820.1:c.1144+2890G>T | ENSP00000514621.1:n.1144+2890G>T | |
| ENST00000699821.1:c.1450G>T | ENSP00000514622.1:p.Asp484Tyr | |
| ENST00000699822.1:c.*1307G>T | ENSP00000514623.1:n.*1307G>T | |
| ENST00000699823.1:c.1450G>T | ENSP00000514624.1:p.Asp484Tyr | |
| ENST00000699824.1:c.*1358G>T | ENSP00000514625.1:n.*1358G>T | |
| ENST00000699825.1:c.1294G>T | ENSP00000514626.1:p.Asp432Tyr | |
| ENST00000699826.1:c.*1254G>T | ENSP00000514627.1:n.*1254G>T | |
| ENST00000699827.1:c.1687G>T | ENSP00000514628.1:p.Asp563Tyr | |
| ENST00000699828.1:c.*945G>T | ENSP00000514629.1:n.*945G>T | |
| ENST00000699833.1:n.3627G>T | ||
| ENST00000699837.1:c.1450G>T | ENSP00000514635.1:p.Asp484Tyr | |
| ENST00000699838.1:c.*1755G>T | ENSP00000514636.1:n.*1755G>T | |
| ENST00000699839.1:c.2041G>T | ENSP00000514637.1:p.Asp681Tyr | |
| ENST00000699916.1:c.*1112G>T | ENSP00000514684.1:n.*1112G>T | |
| ENST00000699917.1:c.*1304G>T | ENSP00000514685.1:n.*1304G>T | |
| ENST00000699918.1:c.*1356G>T | ENSP00000514686.1:n.*1356G>T | |
| ENST00000699919.1:c.*1442G>T | ENSP00000514687.1:n.*1442G>T | |
| ENST00000699920.1:c.*1491G>T | ENSP00000514688.1:n.*1491G>T | |
| ENST00000699928.1:c.989-3919G>T | ENSP00000514693.1:n.989-3919G>T | |
| ENST00000699951.1:c.*951G>T | ENSP00000514706.1:n.*951G>T | |
| ENST00000699952.1:c.803+10416G>T | ENSP00000514707.1:n.803+10416G>T | |
| ENST00000265849.12:c.1855G>T MANE Select | ENSP00000265849.7:p.Asp619Tyr | |
| ENST00000642292.1:c.1450G>T | ENSP00000495524.1:p.Asp484Tyr | |
| ENST00000642456.1:c.1450G>T | ENSP00000493814.1:p.Asp484Tyr | |
| ENST00000643595.1:c.*1254G>T | ENSP00000494497.1:n.*1254G>T | |
| ENST00000644110.1:c.1537G>T | ENSP00000496392.1:p.Asp513Tyr | |
| ENST00000265849.11:c.1855G>T | ENSP00000265849.7:p.Asp619Tyr | |
| ENST00000382321.5:c.804-3919G>T | ENSP00000371758.4:n.804-3919G>T | |
| ENST00000406569.7:n.1678+177G>T | ||
| ENST00000441476.6:c.1537G>T | ENSP00000392843.2:p.Asp513Tyr | |
| ENST00000469652.1:n.63-4005G>T | ||
| NM_000535.5:c.1855G>T , LRG_161t1:c.1855G>T | NP_000526.1:p.Asp619Tyr | |
| NR_003085.2:n.1937G>T | ||
| XM_006715742.2:c.1849G>T | XP_006715805.1:p.Asp617Tyr | |
| XM_006715744.2:c.922G>T | XP_006715807.1:p.Asp308Tyr | |
| XM_011515427.1:c.1900G>T | XP_011513729.1:p.Asp634Tyr | |
| XM_011515428.1:c.1744G>T | XP_011513730.1:p.Asp582Tyr | |
| XM_011515429.1:c.1537G>T | XP_011513731.1:p.Asp513Tyr | |
| XM_011515430.1:c.1537G>T | XP_011513732.1:p.Asp513Tyr | |
| NM_000535.6:c.1855G>T | NP_000526.2:p.Asp619Tyr | |
| NM_001322003.1:c.1450G>T | NP_001308932.1:p.Asp484Tyr | |
| NM_001322004.1:c.1450G>T | NP_001308933.1:p.Asp484Tyr | |
| NM_001322005.1:c.1450G>T | NP_001308934.1:p.Asp484Tyr | |
| NM_001322006.1:c.1699G>T | NP_001308935.1:p.Asp567Tyr | |
| NM_001322007.1:c.1537G>T | NP_001308936.1:p.Asp513Tyr | |
| NM_001322008.1:c.1537G>T | NP_001308937.1:p.Asp513Tyr | |
| NM_001322009.1:c.1450G>T | NP_001308938.1:p.Asp484Tyr | |
| NM_001322010.1:c.1294G>T | NP_001308939.1:p.Asp432Tyr | |
| NM_001322011.1:c.922G>T | NP_001308940.1:p.Asp308Tyr | |
| NM_001322012.1:c.922G>T | NP_001308941.1:p.Asp308Tyr | |
| NM_001322013.1:c.1282G>T | NP_001308942.1:p.Asp428Tyr | |
| NM_001322014.1:c.1855G>T | NP_001308943.1:p.Asp619Tyr | |
| NM_001322015.1:c.1546G>T | NP_001308944.1:p.Asp516Tyr | |
| NR_136154.1:n.1942G>T | ||
| XM_006715744.4:c.922G>T | XP_006715807.1:p.Asp308Tyr | |
| XM_017012342.2:c.922G>T | XP_016867831.1:p.Asp308Tyr | |
| XM_024446800.1:c.1294G>T | XP_024302568.1:p.Asp432Tyr | |
| NM_000535.7:c.1855G>T MANE Select | NP_000526.2:p.Asp619Tyr | |
| NM_001322003.2:c.1450G>T | NP_001308932.1:p.Asp484Tyr | |
| NM_001322004.2:c.1450G>T | NP_001308933.1:p.Asp484Tyr | |
| NM_001322005.2:c.1450G>T | NP_001308934.1:p.Asp484Tyr | |
| NM_001322006.2:c.1699G>T | NP_001308935.1:p.Asp567Tyr | |
| NM_001322008.2:c.1537G>T | NP_001308937.1:p.Asp513Tyr | |
| NM_001322009.2:c.1450G>T | NP_001308938.1:p.Asp484Tyr | |
| NM_001322010.2:c.1294G>T | NP_001308939.1:p.Asp432Tyr | |
| NM_001322011.2:c.922G>T | NP_001308940.1:p.Asp308Tyr | |
| NM_001322012.2:c.922G>T | NP_001308941.1:p.Asp308Tyr | |
| NM_001322013.2:c.1282G>T | NP_001308942.1:p.Asp428Tyr | |
| NM_001322014.2:c.1855G>T | NP_001308943.1:p.Asp619Tyr | |
| NM_001322015.2:c.1546G>T | NP_001308944.1:p.Asp516Tyr | |
| NM_001322007.2:c.1537G>T | NP_001308936.1:p.Asp513Tyr |