Canonical Allele Identifier: CA375262997

Gene: ABL1

Linked Data

• MyVariant Identifiers: chr9:g.133738313A>T (hg19) ; chr9:g.130862926A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130862926A>T , CM000671.2:g.130862926A>T	GRCh38
NC_000009.11:g.133738313A>T , CM000671.1:g.133738313A>T	GRCh37
NC_000009.10:g.132728134A>T	NCBI36
NG_012034.1:g.154046A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000372348.9:c.770A>T	ENSP00000361423.2:p.Glu257Val
ENST00000318560.6:c.713A>T MANE Select	ENSP00000323315.5:p.Glu238Val
ENST00000372348.7:c.770A>T	ENSP00000361423.2:p.Glu257Val
ENST00000318560.5:c.713A>T	ENSP00000323315.5:p.Glu238Val
ENST00000372348.6:c.770A>T	ENSP00000361423.2:p.Glu257Val
NM_005157.5:c.713A>T	NP_005148.2:p.Glu238Val
NM_007313.2:c.770A>T	NP_009297.2:p.Glu257Val
NM_005157.6:c.713A>T MANE Select	NP_005148.2:p.Glu238Val
NM_007313.3:c.770A>T	NP_009297.2:p.Glu257Val