Linked Data
ClinVar Variation Id:
1116310
dbSNP Id:
rs1272384074
gnomAD v2:
11-17408670-G-A
gnomAD v3:
11-17387123-G-A
gnomAD v4:
11-17387123-G-A
COSMIC:
COSM6452313
MyVariant Identifiers:
chr11:g.17408670G>A (hg19)
chr11:g.17408670_17408673delinsATCC (hg19)
chr11:g.17387123G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17387123G>A , CM000673.2:g.17387123G>A | GRCh38 |
| NC_000011.9:g.17408670G>A , CM000673.1:g.17408670G>A | GRCh37 |
| NC_000011.8:g.17365246G>A | NCBI36 |
| NG_012446.1:g.6537C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682350.1:c.708C>T | ENSP00000508090.1:p.Asp236= | |
| ENST00000682764.1:c.708C>T | ENSP00000506780.1:p.Asp236= | |
| ENST00000339994.5:c.969C>T MANE Select | ENSP00000345708.4:p.Asp323= | |
| ENST00000339994.4:c.969C>T | ENSP00000345708.4:p.Asp323= | |
| ENST00000528731.1:c.708C>T | ENSP00000434755.1:p.Asp236= | |
| NM_000525.3:c.969C>T | NP_000516.3:p.Asp323= | |
| NM_001166290.1:c.708C>T | NP_001159762.1:p.Asp236= | |
| XM_006718226.2:c.708C>T | XP_006718289.1:p.Asp236= | |
| XR_930867.1:n.1127C>T | ||
| XM_006718226.3:c.708C>T | XP_006718289.1:p.Asp236= | |
| XM_017017680.1:c.708C>T | XP_016873169.1:p.Asp236= | |
| NM_001166290.2:c.708C>T | NP_001159762.1:p.Asp236= | |
| NM_001377296.1:c.708C>T | NP_001364225.1:p.Asp236= | |
| NM_001377297.1:c.708C>T | NP_001364226.1:p.Asp236= | |
| NM_000525.4:c.969C>T MANE Select | NP_000516.3:p.Asp323= |