Canonical Allele Identifier: CA1881463031
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862795C= , CM000671.2:g.130862795C= GRCh38
NC_000009.11:g.133738182C= , CM000671.1:g.133738182C= GRCh37
NC_000009.10:g.132728003C= NCBI36
NG_012034.1:g.153915C=

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.639C= ENSP00000361423.2:p.Thr213=
ENST00000318560.6:c.582C= MANE Select ENSP00000323315.5:p.Thr194=
ENST00000372348.7:c.639C= ENSP00000361423.2:p.Thr213=
ENST00000318560.5:c.582C= ENSP00000323315.5:p.Thr194=
ENST00000372348.6:c.639C= ENSP00000361423.2:p.Thr213=
NM_005157.5:c.582C= NP_005148.2:p.Thr194=
NM_007313.2:c.639C= NP_009297.2:p.Thr213=
NM_005157.6:c.582C= MANE Select NP_005148.2:p.Thr194=
NM_007313.3:c.639C= NP_009297.2:p.Thr213=