Canonical Allele Identifier: CA2500527852
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872432_130872436del , CM000671.2:g.130872432_130872436del GRCh38
NC_000009.11:g.133747819_133747823del , CM000671.1:g.133747819_133747823del GRCh37
NC_000009.10:g.132737640_132737644del NCBI36
NG_012034.1:g.163552_163556del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.964+219_964+223del ENSP00000361423.2:n.964+219_964+223del
ENST00000318560.6:c.907+219_907+223del MANE Select ENSP00000323315.5:n.907+219_907+223del
ENST00000372348.7:c.964+219_964+223del ENSP00000361423.2:n.964+219_964+223del
ENST00000318560.5:c.907+219_907+223del ENSP00000323315.5:n.907+219_907+223del
ENST00000372348.6:c.964+219_964+223del ENSP00000361423.2:n.964+219_964+223del
NM_005157.5:c.907+219_907+223del NP_005148.2:n.907+219_907+223del
NM_007313.2:c.964+219_964+223del NP_009297.2:n.964+219_964+223del
NM_005157.6:c.907+219_907+223del MANE Select NP_005148.2:n.907+219_907+223del
NM_007313.3:c.964+219_964+223del NP_009297.2:n.964+219_964+223del