Linked Data
ClinVar Variation Id:
833804
ClinVar RCV Id:
RCV001034312
dbSNP Id:
rs1832220041
gnomAD v4:
9-135765729-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.135765729G>A , CM000671.2:g.135765729G>A | GRCh38 |
| NC_000009.11:g.138657575G>A , CM000671.1:g.138657575G>A | GRCh37 |
| NC_000009.10:g.137797396G>A | NCBI36 |
| NG_033070.1:g.68545G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371757.7:c.1306G>A MANE Select | ENSP00000360822.2:p.Ala436Thr | |
| ENST00000636995.1:n.33G>A | ||
| ENST00000637798.1:n.45G>A | ||
| ENST00000674572.1:c.1147G>A | ENSP00000501742.1:p.Ala383Thr | |
| ENST00000675090.1:c.1054G>A | ENSP00000501833.1:p.Ala352Thr | |
| ENST00000675399.1:c.1054G>A | ENSP00000501932.1:p.Ala352Thr | |
| ENST00000676421.1:c.1063G>A | ENSP00000502322.1:p.Ala355Thr | |
| ENST00000263604.5:c.1207G>A | ENSP00000263604.4:p.Ala403Thr | |
| ENST00000371757.6:c.1306G>A | ENSP00000360822.2:p.Ala436Thr | |
| ENST00000460750.5:c.*916G>A | ENSP00000418777.1:n.*916G>A | |
| ENST00000486577.6:c.1189G>A | ENSP00000417578.3:p.Ala397Thr | |
| ENST00000487664.5:c.1306G>A | ENSP00000417851.2:p.Ala436Thr | |
| ENST00000488444.6:c.1249G>A | ENSP00000419007.3:p.Ala417Thr | |
| ENST00000490355.6:c.1249G>A | ENSP00000418003.3:p.Ala417Thr | |
| ENST00000490363.3:n.1125G>A | ||
| ENST00000491806.6:c.1249G>A | ENSP00000419086.3:p.Ala417Thr | |
| ENST00000628528.2:c.1171G>A | ENSP00000486374.1:p.Ala391Thr | |
| ENST00000630792.2:c.1147G>A | ENSP00000486486.1:p.Ala383Thr | |
| ENST00000631073.2:c.1249G>A | ENSP00000486130.1:p.Ala417Thr | |
| NM_001272003.1:c.1171G>A | NP_001258932.1:p.Ala391Thr | |
| NM_020822.2:c.1306G>A | NP_065873.2:p.Ala436Thr | |
| XM_011518877.1:c.1441G>A | XP_011517179.1:p.Ala481Thr | |
| XM_011518878.1:c.1450G>A | XP_011517180.1:p.Ala484Thr | |
| XM_011518879.1:c.1441G>A | XP_011517181.1:p.Ala481Thr | |
| XM_011518880.1:c.1207G>A | XP_011517182.1:p.Ala403Thr | |
| XM_011518881.1:c.796G>A | XP_011517183.1:p.Ala266Thr | |
| XM_011518877.3:c.1441G>A | XP_011517179.1:p.Ala481Thr | |
| XM_011518878.3:c.1450G>A | XP_011517180.1:p.Ala484Thr | |
| XM_011518879.3:c.1441G>A | XP_011517181.1:p.Ala481Thr | |
| XM_011518881.3:c.796G>A | XP_011517183.1:p.Ala266Thr | |
| XM_017014931.1:c.1240G>A | XP_016870420.1:p.Ala414Thr | |
| XM_017014932.1:c.1063G>A | XP_016870421.1:p.Ala355Thr | |
| XM_017014933.1:c.796G>A | XP_016870422.1:p.Ala266Thr | |
| XM_024447617.1:c.796G>A | XP_024303385.1:p.Ala266Thr | |
| XM_024447618.1:c.796G>A | XP_024303386.1:p.Ala266Thr | |
| NM_020822.3:c.1306G>A MANE Select | NP_065873.2:p.Ala436Thr | |
| NM_001272003.2:c.1171G>A | NP_001258932.1:p.Ala391Thr |