Canonical Allele Identifier: CA645556977
Gene: ABL1 HGNC NCBI

Linked Data

COSMIC: COSM86990

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872190_130872192dup , CM000671.2:g.130872190_130872192dup GRCh38
NC_000009.11:g.133747577_133747579dup , CM000671.1:g.133747577_133747579dup GRCh37
NC_000009.10:g.132737398_132737400dup NCBI36
NG_012034.1:g.163310_163312dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.941_943dup ENSP00000361423.2:p.His314_Pro315insHis
ENST00000318560.6:c.884_886dup MANE Select ENSP00000323315.5:p.His295_Pro296insHis
ENST00000372348.7:c.941_943dup ENSP00000361423.2:p.His314_Pro315insHis
ENST00000318560.5:c.884_886dup ENSP00000323315.5:p.His295_Pro296insHis
ENST00000372348.6:c.941_943dup ENSP00000361423.2:p.His314_Pro315insHis
NM_005157.5:c.884_886dup NP_005148.2:p.His295_Pro296insHis
NM_007313.2:c.941_943dup NP_009297.2:p.His314_Pro315insHis
NM_005157.6:c.884_886dup MANE Select NP_005148.2:p.His295_Pro296insHis
NM_007313.3:c.941_943dup NP_009297.2:p.His314_Pro315insHis