Canonical Allele Identifier: CA375262503

Gene: ABL1

Linked Data

• dbSNP Id: rs2132973528
• MyVariant Identifiers: chr9:g.133738220A>C (hg19) ; chr9:g.130862833A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130862833A>C , CM000671.2:g.130862833A>C	GRCh38
NC_000009.11:g.133738220A>C , CM000671.1:g.133738220A>C	GRCh37
NC_000009.10:g.132728041A>C	NCBI36
NG_012034.1:g.153953A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.677A>C	ENSP00000361423.2:p.Asp226Ala
ENST00000318560.6:c.620A>C MANE Select	ENSP00000323315.5:p.Asp207Ala
ENST00000372348.7:c.677A>C	ENSP00000361423.2:p.Asp226Ala
ENST00000318560.5:c.620A>C	ENSP00000323315.5:p.Asp207Ala
ENST00000372348.6:c.677A>C	ENSP00000361423.2:p.Asp226Ala
NM_005157.5:c.620A>C	NP_005148.2:p.Asp207Ala
NM_007313.2:c.677A>C	NP_009297.2:p.Asp226Ala
NM_005157.6:c.620A>C MANE Select	NP_005148.2:p.Asp207Ala
NM_007313.3:c.677A>C	NP_009297.2:p.Asp226Ala