Canonical Allele Identifier: CA1881463508
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862975G= , CM000671.2:g.130862975G= GRCh38
NC_000009.11:g.133738362G= , CM000671.1:g.133738362G= GRCh37
NC_000009.10:g.132728183G= NCBI36
NG_012034.1:g.154095G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.819G= ENSP00000361423.2:p.Gly273=
ENST00000318560.6:c.762G= MANE Select ENSP00000323315.5:p.Gly254=
ENST00000372348.7:c.819G= ENSP00000361423.2:p.Gly273=
ENST00000318560.5:c.762G= ENSP00000323315.5:p.Gly254=
ENST00000372348.6:c.819G= ENSP00000361423.2:p.Gly273=
NM_005157.5:c.762G= NP_005148.2:p.Gly254=
NM_007313.2:c.819G= NP_009297.2:p.Gly273=
NM_005157.6:c.762G= MANE Select NP_005148.2:p.Gly254=
NM_007313.3:c.819G= NP_009297.2:p.Gly273=