Canonical Allele Identifier: CA200680389

Gene: ABL1

Linked Data

• dbSNP Id: rs79052735
• MyVariant Identifiers: chr9:g.133738159T>C (hg19) ; chr9:g.130862772T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130862772T>C , CM000671.2:g.130862772T>C	GRCh38
NC_000009.11:g.133738159T>C , CM000671.1:g.133738159T>C	GRCh37
NC_000009.10:g.132727980T>C	NCBI36
NG_012034.1:g.153892T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000372348.9:c.616T>C	ENSP00000361423.2:p.Ser206Pro
ENST00000318560.6:c.559T>C MANE Select	ENSP00000323315.5:p.Ser187Pro
ENST00000372348.7:c.616T>C	ENSP00000361423.2:p.Ser206Pro
ENST00000318560.5:c.559T>C	ENSP00000323315.5:p.Ser187Pro
ENST00000372348.6:c.616T>C	ENSP00000361423.2:p.Ser206Pro
NM_005157.5:c.559T>C	NP_005148.2:p.Ser187Pro
NM_007313.2:c.616T>C	NP_009297.2:p.Ser206Pro
NM_005157.6:c.559T>C MANE Select	NP_005148.2:p.Ser187Pro
NM_007313.3:c.616T>C	NP_009297.2:p.Ser206Pro