Canonical Allele Identifier: CA1881475722
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872656T= , CM000671.2:g.130872656T= GRCh38
NC_000009.11:g.133748043T= , CM000671.1:g.133748043T= GRCh37
NC_000009.10:g.132737864T= NCBI36
NG_012034.1:g.163776T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.965-204T= ENSP00000361423.2:n.965-204T=
ENST00000318560.6:c.908-204T= MANE Select ENSP00000323315.5:n.908-204T=
ENST00000372348.7:c.965-204T= ENSP00000361423.2:n.965-204T=
ENST00000318560.5:c.908-204T= ENSP00000323315.5:n.908-204T=
ENST00000372348.6:c.965-204T= ENSP00000361423.2:n.965-204T=
NM_005157.5:c.908-204T= NP_005148.2:n.908-204T=
NM_007313.2:c.965-204T= NP_009297.2:n.965-204T=
NM_005157.6:c.908-204T= MANE Select NP_005148.2:n.908-204T=
NM_007313.3:c.965-204T= NP_009297.2:n.965-204T=