Canonical Allele Identifier: CA16602556

Gene: ABL1

Linked Data

• ClinVar Variation Id: 376095
• ClinVar RCV Id: RCV000427169
• dbSNP Id: rs121913450
• COSMIC: COSM12611
• MyVariant Identifiers: chr9:g.133748403A>G (hg19) ; chr9:g.130873016A>G (hg38)
• PubMed: PMID:12399961 ; PMID:12623848 ; PMID:12783380 ; PMID:20010464 ; PMID:20702476 ; PMID:23676790 ; PMID:24456693 ; PMID:25157968
• CIViC: CA16602556

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
ENST00000372348.9:c.1121A>G	ENSP00000361423.2:p.Glu374Gly
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