Linked Data
ClinVar Variation Id:
1433835
ClinVar RCV Id:
RCV001952740
dbSNP Id:
rs773233738
ExAC:
10:88476332 G / A
gnomAD v2:
10-88476332-G-A
gnomAD v3:
10-86716575-G-A
gnomAD v4:
10-86716575-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.86716575G>A , CM000672.2:g.86716575G>A | GRCh38 |
| NC_000010.10:g.88476332G>A , CM000672.1:g.88476332G>A | GRCh37 |
| NC_000010.9:g.88466312G>A | NCBI36 |
| NG_008876.1:g.53012G>A , LRG_385:g.53012G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000687154.1:n.515-2152G>A | ||
| ENST00000688001.1:c.1291G>A | ENSP00000508987.1:p.Asp431Asn | |
| ENST00000689296.1:c.1291G>A | ENSP00000510609.1:p.Asp431Asn | |
| ENST00000689740.1:c.1339G>A | ENSP00000510300.1:p.Asp447Asn | |
| ENST00000693680.1:c.1339G>A | ENSP00000509539.1:p.Asp447Asn | |
| ENST00000361373.9:c.1480G>A MANE Select | ENSP00000355296.3:p.Asp494Asn | |
| ENST00000429277.7:c.1150G>A | ENSP00000401437.3:p.Asp384Asn | |
| ENST00000623056.4:c.1495G>A | ENSP00000485500.1:p.Asp499Asn | |
| ENST00000263066.10:c.1150G>A | ENSP00000263066.6:p.Asp384Asn | |
| ENST00000361373.8:c.1480G>A | ENSP00000355296.3:p.Asp494Asn | |
| ENST00000429277.6:c.1495G>A | ENSP00000401437.2:p.Asp499Asn | |
| ENST00000623056.3:c.1495G>A | ENSP00000485500.1:p.Asp499Asn | |
| NM_001080114.1:c.1150G>A | NP_001073583.1:p.Asp384Asn | |
| NM_001171610.1:c.1495G>A | NP_001165081.1:p.Asp499Asn | |
| NM_007078.2:c.1480G>A , LRG_385t1:c.1480G>A | NP_009009.1:p.Asp494Asn | |
| XM_005269464.3:c.1480G>A | XP_005269521.1:p.Asp494Asn | |
| XM_005269466.3:c.1291G>A | XP_005269523.1:p.Asp431Asn | |
| XM_011539184.1:c.1732G>A | XP_011537486.1:p.Asp578Asn | |
| XM_011539185.1:c.1732G>A | XP_011537487.1:p.Asp578Asn | |
| XM_011539186.1:c.1684G>A | XP_011537488.1:p.Asp562Asn | |
| XM_011539187.1:c.1543G>A | XP_011537489.1:p.Asp515Asn | |
| XM_011539188.1:c.1528G>A | XP_011537490.1:p.Asp510Asn | |
| XM_011539189.1:c.1387G>A | XP_011537491.1:p.Asp463Asn | |
| XM_011539190.1:c.1339G>A | XP_011537492.1:p.Asp447Asn | |
| XM_011539191.1:c.1198G>A | XP_011537493.1:p.Asp400Asn | |
| XM_011539192.1:c.1183G>A | XP_011537494.1:p.Asp395Asn | |
| XM_011539193.1:c.688G>A | XP_011537495.1:p.Asp230Asn | |
| XM_011539194.1:c.499G>A | XP_011537496.1:p.Asp167Asn | |
| XM_005269464.4:c.1480G>A | XP_005269521.1:p.Asp494Asn | |
| XM_005269466.4:c.1291G>A | XP_005269523.1:p.Asp431Asn | |
| XM_011539184.2:c.1732G>A | XP_011537486.1:p.Asp578Asn | |
| XM_011539185.2:c.1732G>A | XP_011537487.1:p.Asp578Asn | |
| XM_011539186.2:c.1684G>A | XP_011537488.1:p.Asp562Asn | |
| XM_011539187.2:c.1543G>A | XP_011537489.1:p.Asp515Asn | |
| XM_011539188.2:c.1528G>A | XP_011537490.1:p.Asp510Asn | |
| XM_011539190.2:c.1339G>A | XP_011537492.1:p.Asp447Asn | |
| XM_011539191.2:c.1198G>A | XP_011537493.1:p.Asp400Asn | |
| XM_017015606.1:c.1528G>A | XP_016871095.1:p.Asp510Asn | |
| XM_017015607.1:c.688G>A | XP_016871096.1:p.Asp230Asn | |
| XM_024447785.1:c.1387G>A | XP_024303553.1:p.Asp463Asn | |
| XM_024447786.1:c.1150G>A | XP_024303554.1:p.Asp384Asn | |
| NM_001080114.2:c.1150G>A | NP_001073583.1:p.Asp384Asn | |
| NM_001171610.2:c.1495G>A | NP_001165081.1:p.Asp499Asn | |
| NM_001368064.1:c.1291G>A | NP_001354993.1:p.Asp431Asn | |
| NM_001368065.1:c.1291G>A | NP_001354994.1:p.Asp431Asn | |
| NM_001368066.1:c.1339G>A | NP_001354995.1:p.Asp447Asn | |
| NM_007078.3:c.1480G>A MANE Select | NP_009009.1:p.Asp494Asn |