Canonical Allele Identifier: CA375249349

Gene: ABL1

Linked Data

• MyVariant Identifiers: chr9:g.133748250T>C (hg19) ; chr9:g.130872863T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872863T>C , CM000671.2:g.130872863T>C	GRCh38
NC_000009.11:g.133748250T>C , CM000671.1:g.133748250T>C	GRCh37
NC_000009.10:g.132738071T>C	NCBI36
NG_012034.1:g.163983T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000372348.9:c.968T>C	ENSP00000361423.2:p.Val323Ala
ENST00000318560.6:c.911T>C MANE Select	ENSP00000323315.5:p.Val304Ala
ENST00000372348.7:c.968T>C	ENSP00000361423.2:p.Val323Ala
ENST00000318560.5:c.911T>C	ENSP00000323315.5:p.Val304Ala
ENST00000372348.6:c.968T>C	ENSP00000361423.2:p.Val323Ala
NM_005157.5:c.911T>C	NP_005148.2:p.Val304Ala
NM_007313.2:c.968T>C	NP_009297.2:p.Val323Ala
NM_005157.6:c.911T>C MANE Select	NP_005148.2:p.Val304Ala
NM_007313.3:c.968T>C	NP_009297.2:p.Val323Ala