Canonical Allele Identifier: CA467394978

Gene: ABL1

Linked Data

• MyVariant Identifiers: chr9:g.133747557A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872170A>C , CM000671.2:g.130872170A>C	GRCh38
NC_000009.11:g.133747557A>C , CM000671.1:g.133747557A>C	GRCh37
NC_000009.10:g.132737378A>C	NCBI36
NG_012034.1:g.163290A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.921A>C	ENSP00000361423.2:p.Ala307=
ENST00000318560.6:c.864A>C MANE Select	ENSP00000323315.5:p.Ala288=
ENST00000372348.7:c.921A>C	ENSP00000361423.2:p.Ala307=
ENST00000318560.5:c.864A>C	ENSP00000323315.5:p.Ala288=
ENST00000372348.6:c.921A>C	ENSP00000361423.2:p.Ala307=
NM_005157.5:c.864A>C	NP_005148.2:p.Ala288=
NM_007313.2:c.921A>C	NP_009297.2:p.Ala307=
NM_005157.6:c.864A>C MANE Select	NP_005148.2:p.Ala288=
NM_007313.3:c.921A>C	NP_009297.2:p.Ala307=