Canonical Allele Identifier: CA16602556
Gene: ABL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 376095
ClinVar RCV Id: RCV000427169
dbSNP Id: rs121913450
COSMIC: COSM12611

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130873016A>G , CM000671.2:g.130873016A>G GRCh38
NC_000009.11:g.133748403A>G , CM000671.1:g.133748403A>G GRCh37
NC_000009.10:g.132738224A>G NCBI36
NG_012034.1:g.164136A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000318560.6:c.1064A>G MANE Select ENSP00000323315.5:p.Glu355Gly
ENST00000372348.7:c.1121A>G ENSP00000361423.2:p.Glu374Gly
ENST00000318560.5:c.1064A>G ENSP00000323315.5:p.Glu355Gly
ENST00000372348.6:c.1121A>G ENSP00000361423.2:p.Glu374Gly
NM_005157.5:c.1064A>G NP_005148.2:p.Glu355Gly
NM_007313.2:c.1121A>G NP_009297.2:p.Glu374Gly
NM_005157.6:c.1064A>G MANE Select NP_005148.2:p.Glu355Gly
NM_007313.3:c.1121A>G NP_009297.2:p.Glu374Gly