Canonical Allele Identifier: CA375263022

Gene: ABL1

Linked Data

• MyVariant Identifiers: chr9:g.133738316G>C (hg19) ; chr9:g.130862929G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130862929G>C , CM000671.2:g.130862929G>C	GRCh38
NC_000009.11:g.133738316G>C , CM000671.1:g.133738316G>C	GRCh37
NC_000009.10:g.132728137G>C	NCBI36
NG_012034.1:g.154049G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000372348.9:c.773G>C	ENSP00000361423.2:p.Arg258Pro
ENST00000318560.6:c.716G>C MANE Select	ENSP00000323315.5:p.Arg239Pro
ENST00000372348.7:c.773G>C	ENSP00000361423.2:p.Arg258Pro
ENST00000318560.5:c.716G>C	ENSP00000323315.5:p.Arg239Pro
ENST00000372348.6:c.773G>C	ENSP00000361423.2:p.Arg258Pro
NM_005157.5:c.716G>C	NP_005148.2:p.Arg239Pro
NM_007313.2:c.773G>C	NP_009297.2:p.Arg258Pro
NM_005157.6:c.716G>C MANE Select	NP_005148.2:p.Arg239Pro
NM_007313.3:c.773G>C	NP_009297.2:p.Arg258Pro