Canonical Allele Identifier: CA122578
Gene: ABL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 12625
ClinVar RCV Id: RCV000013460
dbSNP Id: rs387906516

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862920A>T , CM000671.2:g.130862920A>T GRCh38
NC_000009.11:g.133738307A>T , CM000671.1:g.133738307A>T GRCh37
NC_000009.10:g.132728128A>T NCBI36
NG_012034.1:g.154040A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.764A>T ENSP00000361423.2:p.Glu255Val
ENST00000318560.6:c.707A>T MANE Select ENSP00000323315.5:p.Glu236Val
ENST00000372348.7:c.764A>T ENSP00000361423.2:p.Glu255Val
ENST00000318560.5:c.707A>T ENSP00000323315.5:p.Glu236Val
ENST00000372348.6:c.764A>T ENSP00000361423.2:p.Glu255Val
NM_005157.5:c.707A>T NP_005148.2:p.Glu236Val
NM_007313.2:c.764A>T NP_009297.2:p.Glu255Val
NM_005157.6:c.707A>T MANE Select NP_005148.2:p.Glu236Val
NM_007313.3:c.764A>T NP_009297.2:p.Glu255Val