Linked Data
ClinVar Variation Id:
404159
ClinVar RCV Id:
RCV000462562
dbSNP Id:
rs9651492
COSMIC:
COSM5083
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87933216G>A , CM000672.2:g.87933216G>A | GRCh38 |
| NC_000010.10:g.89692973G>A , CM000672.1:g.89692973G>A | GRCh37 |
| NC_000010.9:g.89682953G>A | NCBI36 |
| NG_007466.2:g.74778G>A , LRG_311:g.74778G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000700029.2:c.457G>A | ENSP00000514759.2:p.Asp153Asn | |
| ENST00000710265.1:c.457G>A | ENSP00000518161.1:p.Asp153Asn | |
| ENST00000472832.3:c.457G>A | ENSP00000483066.2:p.Asp153Asn | |
| ENST00000688158.2:n.1192G>A | ||
| ENST00000688922.2:c.*287G>A | ENSP00000508742.2:n.*287G>A | |
| ENST00000700021.1:c.412G>A | ENSP00000514757.1:p.Asp138Asn | |
| ENST00000700022.1:c.457G>A | ENSP00000514758.1:p.Asp153Asn | |
| ENST00000700029.1:c.291G>A | ||
| ENST00000706954.1:c.457G>A | ENSP00000516674.1:p.Asp153Asn | |
| ENST00000706955.1:c.*492G>A | ENSP00000516675.1:n.*492G>A | |
| ENST00000686459.1:c.457G>A | ENSP00000508909.1:p.Asp153Asn | |
| ENST00000688158.1:c.*568G>A | ENSP00000509254.1:n.*568G>A | |
| ENST00000688308.1:c.457G>A | ENSP00000508752.1:p.Asp153Asn | |
| ENST00000688922.1:c.378G>A | ||
| ENST00000693560.1:c.976G>A | ENSP00000509861.1:p.Asp326Asn | |
| ENST00000371953.8:c.457G>A MANE Select | ENSP00000361021.3:p.Asp153Asn | |
| ENST00000371953.7:c.457G>A | ENSP00000361021.3:p.Asp153Asn | |
| ENST00000498703.1:n.283G>A | ||
| ENST00000610634.1:c.355G>A | ENSP00000477517.1:p.Asp119Asn | |
| NM_000314.5:c.457G>A | NP_000305.3:p.Asp153Asn | |
| NM_000314.6:c.457G>A | NP_000305.3:p.Asp153Asn | |
| NM_001304717.2:c.976G>A | NP_001291646.2:p.Asp326Asn | |
| NM_001304718.1:c.-294G>A | NP_001291647.1:n.-294G>A | |
| XM_006717926.2:c.412G>A | XP_006717989.1:p.Asp138Asn | |
| XM_011539981.1:c.457G>A | XP_011538283.1:p.Asp153Asn | |
| XM_011539982.1:c.361G>A | XP_011538284.1:p.Asp121Asn | |
| XR_945789.1:n.1169G>A | ||
| XR_945790.1:n.1169G>A | ||
| XR_945791.1:n.1169G>A | ||
| NM_000314.7:c.457G>A | NP_000305.3:p.Asp153Asn | |
| NM_001304717.5:c.976G>A | NP_001291646.4:p.Asp326Asn | |
| NM_001304718.2:c.-294G>A | NP_001291647.1:n.-294G>A | |
| NM_000314.8:c.457G>A MANE Select | NP_000305.3:p.Asp153Asn |