Canonical Allele Identifier: CA375263000

Gene: ABL1

Linked Data

• MyVariant Identifiers: chr9:g.133738314A>C (hg19) ; chr9:g.130862927A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130862927A>C , CM000671.2:g.130862927A>C	GRCh38
NC_000009.11:g.133738314A>C , CM000671.1:g.133738314A>C	GRCh37
NC_000009.10:g.132728135A>C	NCBI36
NG_012034.1:g.154047A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000372348.9:c.771A>C	ENSP00000361423.2:p.Glu257Asp
ENST00000318560.6:c.714A>C MANE Select	ENSP00000323315.5:p.Glu238Asp
ENST00000372348.7:c.771A>C	ENSP00000361423.2:p.Glu257Asp
ENST00000318560.5:c.714A>C	ENSP00000323315.5:p.Glu238Asp
ENST00000372348.6:c.771A>C	ENSP00000361423.2:p.Glu257Asp
NM_005157.5:c.714A>C	NP_005148.2:p.Glu238Asp
NM_007313.2:c.771A>C	NP_009297.2:p.Glu257Asp
NM_005157.6:c.714A>C MANE Select	NP_005148.2:p.Glu238Asp
NM_007313.3:c.771A>C	NP_009297.2:p.Glu257Asp