Linked Data
ClinVar Variation Id:
1383219
ClinVar RCV Id:
RCV001924533
dbSNP Id:
rs1185119035
gnomAD v2:
12-8757811-C-A
gnomAD v4:
12-8605215-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.8605215C>A , CM000674.2:g.8605215C>A | GRCh38 |
| NC_000012.11:g.8757811C>A , CM000674.1:g.8757811C>A | GRCh37 |
| NC_000012.10:g.8649078C>A | NCBI36 |
| NG_011588.1:g.12632G>T , LRG_17:g.12632G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000537228.6:c.427G>T | ENSP00000445691.1:p.Glu143Ter | |
| ENST00000543081.6:c.427G>T | ENSP00000439103.2:p.Ala143Ser | |
| ENST00000544516.6:c.157-878G>T | ENSP00000439538.2:n.157-878G>T | |
| ENST00000545576.2:n.536G>T | ||
| ENST00000696246.1:c.412G>T | ENSP00000512504.1:p.Glu138Ter | |
| ENST00000696271.1:n.547G>T | ||
| ENST00000696272.1:c.412G>T | ENSP00000512515.1:p.Asp138Tyr | |
| ENST00000696273.1:c.460G>T | ENSP00000512516.1:p.Asp154Tyr | |
| ENST00000229335.11:c.427G>T MANE Select | ENSP00000229335.6:p.Asp143Tyr | |
| ENST00000229335.10:c.427G>T | ENSP00000229335.6:p.Asp143Tyr | |
| ENST00000537228.5:c.427G>T | ENSP00000445691.1:p.Glu143Ter | |
| ENST00000543081.5:c.423G>T | ||
| ENST00000544516.5:c.153-878G>T | ||
| ENST00000545512.1:c.423G>T | ||
| ENST00000545576.1:n.461G>T | ||
| NM_020661.2:c.427G>T , LRG_17t1:c.427G>T | NP_065712.1:p.Asp143Tyr | |
| XM_011520772.1:c.427G>T | XP_011519074.1:p.Glu143Ter | |
| XM_011520773.1:c.427G>T | XP_011519075.1:p.Ala143Ser | |
| NM_001330343.1:c.427G>T | NP_001317272.1:p.Glu143Ter | |
| NM_020661.3:c.427G>T | NP_065712.1:p.Asp143Tyr | |
| XM_011520773.2:c.427G>T | XP_011519075.1:p.Ala143Ser | |
| NM_020661.4:c.427G>T MANE Select | NP_065712.1:p.Asp143Tyr | |
| NM_001330343.2:c.427G>T | NP_001317272.1:p.Glu143Ter |