Canonical Allele Identifier: CA1881474978
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872496T= , CM000671.2:g.130872496T= GRCh38
NC_000009.11:g.133747883T= , CM000671.1:g.133747883T= GRCh37
NC_000009.10:g.132737704T= NCBI36
NG_012034.1:g.163616T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.964+283T= ENSP00000361423.2:n.964+283T=
ENST00000318560.6:c.907+283T= MANE Select ENSP00000323315.5:n.907+283T=
ENST00000372348.7:c.964+283T= ENSP00000361423.2:n.964+283T=
ENST00000318560.5:c.907+283T= ENSP00000323315.5:n.907+283T=
ENST00000372348.6:c.964+283T= ENSP00000361423.2:n.964+283T=
NM_005157.5:c.907+283T= NP_005148.2:n.907+283T=
NM_007313.2:c.964+283T= NP_009297.2:n.964+283T=
NM_005157.6:c.907+283T= MANE Select NP_005148.2:n.907+283T=
NM_007313.3:c.964+283T= NP_009297.2:n.964+283T=