Canonical Allele Identifier: CA2579485002
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872243del , CM000671.2:g.130872243del GRCh38
NC_000009.11:g.133747630del , CM000671.1:g.133747630del GRCh37
NC_000009.10:g.132737451del NCBI36
NG_012034.1:g.163363del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.964+30del ENSP00000361423.2:n.964+30del
ENST00000318560.6:c.907+30del MANE Select ENSP00000323315.5:n.907+30del
ENST00000372348.7:c.964+30del ENSP00000361423.2:n.964+30del
ENST00000318560.5:c.907+30del ENSP00000323315.5:n.907+30del
ENST00000372348.6:c.964+30del ENSP00000361423.2:n.964+30del
NM_005157.5:c.907+30del NP_005148.2:n.907+30del
NM_007313.2:c.964+30del NP_009297.2:n.964+30del
NM_005157.6:c.907+30del MANE Select NP_005148.2:n.907+30del
NM_007313.3:c.964+30del NP_009297.2:n.964+30del