Canonical Allele Identifier: CA375262713

Gene: ABL1

Linked Data

• dbSNP Id: rs2132973742
• MyVariant Identifiers: chr9:g.133738267C>A (hg19) ; chr9:g.130862880C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130862880C>A , CM000671.2:g.130862880C>A	GRCh38
NC_000009.11:g.133738267C>A , CM000671.1:g.133738267C>A	GRCh37
NC_000009.10:g.132728088C>A	NCBI36
NG_012034.1:g.154000C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000372348.9:c.724C>A	ENSP00000361423.2:p.Pro242Thr
ENST00000318560.6:c.667C>A MANE Select	ENSP00000323315.5:p.Pro223Thr
ENST00000372348.7:c.724C>A	ENSP00000361423.2:p.Pro242Thr
ENST00000318560.5:c.667C>A	ENSP00000323315.5:p.Pro223Thr
ENST00000372348.6:c.724C>A	ENSP00000361423.2:p.Pro242Thr
NM_005157.5:c.667C>A	NP_005148.2:p.Pro223Thr
NM_007313.2:c.724C>A	NP_009297.2:p.Pro242Thr
NM_005157.6:c.667C>A MANE Select	NP_005148.2:p.Pro223Thr
NM_007313.3:c.724C>A	NP_009297.2:p.Pro242Thr