Canonical Allele Identifier: CA1881463417
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862960C= , CM000671.2:g.130862960C= GRCh38
NC_000009.11:g.133738347C= , CM000671.1:g.133738347C= GRCh37
NC_000009.10:g.132728168C= NCBI36
NG_012034.1:g.154080C=

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.804C= ENSP00000361423.2:p.Gly268=
ENST00000318560.6:c.747C= MANE Select ENSP00000323315.5:p.Gly249=
ENST00000372348.7:c.804C= ENSP00000361423.2:p.Gly268=
ENST00000318560.5:c.747C= ENSP00000323315.5:p.Gly249=
ENST00000372348.6:c.804C= ENSP00000361423.2:p.Gly268=
NM_005157.5:c.747C= NP_005148.2:p.Gly249=
NM_007313.2:c.804C= NP_009297.2:p.Gly268=
NM_005157.6:c.747C= MANE Select NP_005148.2:p.Gly249=
NM_007313.3:c.804C= NP_009297.2:p.Gly268=