Canonical Allele Identifier: CA467395129

Gene: ABL1

Linked Data

• MyVariant Identifiers: chr9:g.133748335G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872948G>C , CM000671.2:g.130872948G>C	GRCh38
NC_000009.11:g.133748335G>C , CM000671.1:g.133748335G>C	GRCh37
NC_000009.10:g.132738156G>C	NCBI36
NG_012034.1:g.164068G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.1053G>C	ENSP00000361423.2:p.Arg351=
ENST00000318560.6:c.996G>C MANE Select	ENSP00000323315.5:p.Arg332=
ENST00000372348.7:c.1053G>C	ENSP00000361423.2:p.Arg351=
ENST00000318560.5:c.996G>C	ENSP00000323315.5:p.Arg332=
ENST00000372348.6:c.1053G>C	ENSP00000361423.2:p.Arg351=
NM_005157.5:c.996G>C	NP_005148.2:p.Arg332=
NM_007313.2:c.1053G>C	NP_009297.2:p.Arg351=
NM_005157.6:c.996G>C MANE Select	NP_005148.2:p.Arg332=
NM_007313.3:c.1053G>C	NP_009297.2:p.Arg351=