Linked Data
ClinVar Variation Id:
387448
dbSNP Id:
rs754991015
ExAC:
13:100953779 T / G
gnomAD v2:
13-100953779-T-G
gnomAD v3:
13-100301525-T-G
gnomAD v4:
13-100301525-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.100301525T>G , CM000675.2:g.100301525T>G | GRCh38 |
| NC_000013.10:g.100953779T>G , CM000675.1:g.100953779T>G | GRCh37 |
| NC_000013.9:g.99751780T>G | NCBI36 |
| NG_008768.1:g.217443T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000376285.6:c.1131T>G MANE Select | ENSP00000365462.1:p.Ala377= | |
| ENST00000636366.1:c.944+28179T>G | ||
| ENST00000636420.1:c.1010T>G | ||
| ENST00000636475.1:c.944+28179T>G | ||
| ENST00000637657.1:c.945-5667T>G | ||
| ENST00000647303.1:c.*913+28179T>G | ENSP00000495663.1:n.*913+28179T>G | |
| ENST00000376279.7:c.1131T>G | ENSP00000365456.3:p.Ala377= | |
| ENST00000376285.5:c.1131T>G | ENSP00000365462.1:p.Ala377= | |
| ENST00000376286.8:c.1053T>G | ENSP00000365463.4:p.Ala351= | |
| ENST00000424527.5:c.31+8271T>G | ENSP00000396050.1:n.31+8271T>G | |
| NM_000282.3:c.1131T>G | NP_000273.2:p.Ala377= | |
| NM_001127692.2:c.1053T>G | NP_001121164.1:p.Ala351= | |
| NM_001178004.1:c.1131T>G | NP_001171475.1:p.Ala377= | |
| XM_005254059.2:c.1131T>G | XP_005254116.1:p.Ala377= | |
| XM_011521093.1:c.1131T>G | XP_011519395.1:p.Ala377= | |
| XR_931615.1:n.1232T>G | ||
| XR_931616.1:n.1232T>G | ||
| NM_001352605.1:c.1131T>G | NP_001339534.1:p.Ala377= | |
| NM_001352606.1:c.1066-1399T>G | NP_001339535.1:n.1066-1399T>G | |
| NM_001352607.1:c.1053T>G | NP_001339536.1:p.Ala351= | |
| NM_001352608.1:c.988-1399T>G | NP_001339537.1:n.988-1399T>G | |
| NM_001352609.1:c.1131T>G | NP_001339538.1:p.Ala377= | |
| NM_001352610.1:c.186T>G | NP_001339539.1:p.Ala62= | |
| NM_001352611.1:c.186T>G | NP_001339540.1:p.Ala62= | |
| NM_001352612.1:c.121-1399T>G | NP_001339541.1:n.121-1399T>G | |
| NR_148027.1:n.1237T>G | ||
| NR_148028.1:n.1237T>G | ||
| NR_148029.1:n.1159T>G | ||
| NR_148030.1:n.1237T>G | ||
| NR_148031.1:n.1237T>G | ||
| XM_017020605.1:c.1131T>G | XP_016876094.1:p.Ala377= | |
| XM_017020606.1:c.1053T>G | XP_016876095.1:p.Ala351= | |
| XM_017020607.1:c.1032T>G | XP_016876096.1:p.Ala344= | |
| XM_017020609.1:c.1032T>G | XP_016876098.1:p.Ala344= | |
| XM_017020611.1:c.1131T>G | XP_016876100.1:p.Ala377= | |
| XM_017020612.1:c.1131T>G | XP_016876101.1:p.Ala377= | |
| XM_017020613.1:c.1131T>G | XP_016876102.1:p.Ala377= | |
| XM_017020615.1:c.1131T>G | XP_016876104.1:p.Ala377= | |
| XM_017020616.1:c.1131T>G | XP_016876105.1:p.Ala377= | |
| XR_001749567.1:n.1232T>G | ||
| XR_001749568.1:n.1232T>G | ||
| XR_001749569.1:n.1232T>G | ||
| XR_001749574.1:n.1083T>G | ||
| XR_001749576.1:n.1166+28179T>G | ||
| XR_001749577.1:n.1166+28179T>G | ||
| NM_000282.4:c.1131T>G MANE Select | NP_000273.2:p.Ala377= | |
| NM_001352605.2:c.1131T>G | NP_001339534.1:p.Ala377= | |
| NM_001352606.2:c.1066-1399T>G | NP_001339535.1:n.1066-1399T>G | |
| NM_001352607.2:c.1053T>G | NP_001339536.1:p.Ala351= | |
| NM_001352608.2:c.988-1399T>G | NP_001339537.1:n.988-1399T>G | |
| NM_001352609.2:c.1131T>G | NP_001339538.1:p.Ala377= | |
| NM_001352610.2:c.186T>G | NP_001339539.1:p.Ala62= | |
| NM_001352611.2:c.186T>G | NP_001339540.1:p.Ala62= | |
| NM_001352612.2:c.121-1399T>G | NP_001339541.1:n.121-1399T>G | |
| NR_148027.2:n.1159T>G | ||
| NR_148028.2:n.1159T>G | ||
| NR_148029.2:n.1081T>G | ||
| NR_148030.2:n.1159T>G | ||
| NR_148031.2:n.1159T>G | ||
| NM_001127692.3:c.1053T>G | NP_001121164.1:p.Ala351= | |
| NM_001178004.2:c.1131T>G | NP_001171475.1:p.Ala377= |