Linked Data
ClinVar Variation Id:
907344
ClinVar RCV Id:
RCV001157115
dbSNP Id:
rs1380121460
gnomAD v2:
6-135749812-C-A
gnomAD v3:
6-135428674-C-A
gnomAD v4:
6-135428674-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.135428674C>A , CM000668.2:g.135428674C>A | GRCh38 |
| NC_000006.11:g.135749812C>A , CM000668.1:g.135749812C>A | GRCh37 |
| NC_000006.10:g.135791505C>A | NCBI36 |
| NG_008643.1:g.74092G>T | |
| NG_008643.2:g.74092G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000265602.11:c.2578G>T MANE Select | ENSP00000265602.6:p.Ala860Ser | |
| ENST00000367799.7:c.1630G>T | ENSP00000356773.3:p.Ala544Ser | |
| ENST00000527681.2:c.251G>T | ||
| ENST00000679434.1:c.2763G>T | ENSP00000505592.1:n.2763G>T | |
| ENST00000679450.1:c.2578G>T | ENSP00000506494.1:p.Ala860Ser | |
| ENST00000679476.1:c.263G>T | ||
| ENST00000679589.1:c.*2606G>T | ENSP00000506644.1:n.*2606G>T | |
| ENST00000679622.1:c.2578G>T | ENSP00000506261.1:p.Ala860Ser | |
| ENST00000679668.1:c.2578G>T | ENSP00000505364.1:p.Ala860Ser | |
| ENST00000679672.1:c.2578G>T | ENSP00000505697.1:p.Ala860Ser | |
| ENST00000679711.1:c.750G>T | ||
| ENST00000679742.1:c.2578G>T | ENSP00000504890.1:p.Ala860Ser | |
| ENST00000679890.1:n.1069G>T | ||
| ENST00000679925.1:c.2578G>T | ENSP00000505502.1:p.Ala860Ser | |
| ENST00000679943.1:c.2578G>T | ENSP00000505663.1:p.Ala860Ser | |
| ENST00000680119.1:c.2533G>T | ENSP00000506403.1:n.2533G>T | |
| ENST00000680184.1:c.2578G>T | ENSP00000506009.1:p.Ala860Ser | |
| ENST00000680278.1:c.2763G>T | ENSP00000506153.1:n.2763G>T | |
| ENST00000680337.1:c.77G>T | ||
| ENST00000680561.1:n.5321G>T | ||
| ENST00000680656.1:c.2578G>T | ENSP00000505297.1:p.Ala860Ser | |
| ENST00000680826.1:c.2763G>T | ENSP00000505224.1:n.2763G>T | |
| ENST00000680840.1:c.2578G>T | ENSP00000505809.1:p.Ala860Ser | |
| ENST00000680965.1:c.*32G>T | ENSP00000505398.1:n.*32G>T | |
| ENST00000681022.1:c.2578G>T | ENSP00000505121.1:p.Ala860Ser | |
| ENST00000681057.1:n.2034G>T | ||
| ENST00000681301.1:c.2425G>T | ENSP00000505093.1:p.Ala809Ser | |
| ENST00000681332.1:n.3095G>T | ||
| ENST00000681340.1:c.2578G>T | ENSP00000505666.1:p.Ala860Ser | |
| ENST00000681365.1:c.2578G>T | ENSP00000506604.1:p.Ala860Ser | |
| ENST00000681477.1:c.*1365G>T | ENSP00000504989.1:n.*1365G>T | |
| ENST00000681488.1:c.2492+1208G>T | ENSP00000505884.1:n.2492+1208G>T | |
| ENST00000681522.1:c.2578G>T | ENSP00000506005.1:p.Ala860Ser | |
| ENST00000681670.1:c.2578G>T | ENSP00000504895.1:p.Ala860Ser | |
| ENST00000681718.1:c.2578G>T | ENSP00000505266.1:p.Ala860Ser | |
| ENST00000681756.1:c.2578G>T | ENSP00000506505.1:p.Ala860Ser | |
| ENST00000681828.1:c.2578G>T | ENSP00000505608.1:p.Ala860Ser | |
| ENST00000681841.1:c.2578G>T | ENSP00000504965.1:p.Ala860Ser | |
| ENST00000681860.1:c.2069G>T | ENSP00000506250.1:n.2069G>T | |
| ENST00000681945.1:n.3046G>T | ||
| ENST00000265602.10:c.2578G>T | ENSP00000265602.6:p.Ala860Ser | |
| ENST00000327035.10:c.2578G>T | ENSP00000322478.6:p.Ala860Ser | |
| ENST00000367799.6:c.1077G>T | ||
| ENST00000367800.8:c.2578G>T | ENSP00000356774.4:p.Ala860Ser | |
| ENST00000457866.6:c.2578G>T | ENSP00000388650.2:p.Ala860Ser | |
| ENST00000475846.6:c.770G>T | ||
| ENST00000531788.5:c.*781G>T | ENSP00000432167.1:n.*781G>T | |
| NM_001134830.1:c.2578G>T | NP_001128302.1:p.Ala860Ser | |
| NM_001134831.1:c.2578G>T | NP_001128303.1:p.Ala860Ser | |
| NM_001134832.1:c.2578G>T | NP_001128304.1:p.Ala860Ser | |
| NM_017651.4:c.2578G>T | NP_060121.3:p.Ala860Ser | |
| XM_011535910.1:c.2578G>T | XP_011534212.1:p.Ala860Ser | |
| XM_011535911.1:c.2578G>T | XP_011534213.1:p.Ala860Ser | |
| XM_011535912.1:c.2578G>T | XP_011534214.1:p.Ala860Ser | |
| XM_011535913.1:c.2578G>T | XP_011534215.1:p.Ala860Ser | |
| XM_011535914.1:c.2578G>T | XP_011534216.1:p.Ala860Ser | |
| XM_011535915.1:c.2578G>T | XP_011534217.1:p.Ala860Ser | |
| XM_011535916.1:c.2578G>T | XP_011534218.1:p.Ala860Ser | |
| XR_942488.1:n.2871G>T | ||
| XR_942489.1:n.2871G>T | ||
| XR_942490.1:n.2871G>T | ||
| XR_942491.1:n.2871G>T | ||
| XR_942493.1:n.2871G>T | ||
| XR_942494.1:n.2871G>T | ||
| XR_942495.1:n.2871G>T | ||
| NM_001350503.1:c.2578G>T | NP_001337432.1:p.Ala860Ser | |
| NM_001350504.1:c.2578G>T | NP_001337433.1:p.Ala860Ser | |
| XM_011535910.3:c.2578G>T | XP_011534212.1:p.Ala860Ser | |
| XM_011535911.3:c.2578G>T | XP_011534213.1:p.Ala860Ser | |
| XM_017010978.2:c.2578G>T | XP_016866467.1:p.Ala860Ser | |
| XM_017010979.2:c.2578G>T | XP_016866468.1:p.Ala860Ser | |
| XM_017010980.2:c.2578G>T | XP_016866469.1:p.Ala860Ser | |
| XM_017010981.2:c.2524G>T | XP_016866470.1:p.Ala842Ser | |
| XM_017010984.2:c.2578G>T | XP_016866473.1:p.Ala860Ser | |
| XM_024446479.1:c.2524G>T | XP_024302247.1:p.Ala842Ser | |
| XM_024446480.1:c.2578G>T | XP_024302248.1:p.Ala860Ser | |
| XR_001743479.2:n.2968G>T | ||
| XR_001743480.2:n.2968G>T | ||
| XR_001743481.2:n.2968G>T | ||
| XR_001743482.2:n.2968G>T | ||
| XR_001743483.2:n.2968G>T | ||
| XR_001743484.2:n.2968G>T | ||
| XR_001743485.2:n.2968G>T | ||
| XR_001743486.2:n.2968G>T | ||
| XR_001743487.2:n.2968G>T | ||
| XR_001743488.1:n.3210G>T | ||
| XR_001743489.2:n.2968G>T | ||
| XR_001743490.2:n.2968G>T | ||
| XR_002956286.1:n.2849G>T | ||
| XR_002956287.1:n.2849G>T | ||
| NM_001134831.2:c.2578G>T MANE Select | NP_001128303.1:p.Ala860Ser | |
| NM_001134830.2:c.2578G>T | NP_001128302.1:p.Ala860Ser | |
| NM_001134832.2:c.2578G>T | NP_001128304.1:p.Ala860Ser | |
| NM_001350503.2:c.2578G>T | NP_001337432.1:p.Ala860Ser | |
| NM_001350504.2:c.2578G>T | NP_001337433.1:p.Ala860Ser | |
| NM_017651.5:c.2578G>T | NP_060121.3:p.Ala860Ser |