Canonical Allele Identifier: CA1881474968

Gene: ABL1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872487_130872489delinsCTT , CM000671.2:g.130872487_130872489delinsCTT	GRCh38
NC_000009.11:g.133747874_133747876delinsCTT , CM000671.1:g.133747874_133747876delinsCTT	GRCh37
NC_000009.10:g.132737695_132737697delinsCTT	NCBI36
NG_012034.1:g.163607_163609delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.964+274_964+276delinsCTT	ENSP00000361423.2:n.964+274_964+276delinsCTT
ENST00000318560.6:c.907+274_907+276delinsCTT MANE Select	ENSP00000323315.5:n.907+274_907+276delinsCTT
ENST00000372348.7:c.964+274_964+276delinsCTT	ENSP00000361423.2:n.964+274_964+276delinsCTT
ENST00000318560.5:c.907+274_907+276delinsCTT	ENSP00000323315.5:n.907+274_907+276delinsCTT
ENST00000372348.6:c.964+274_964+276delinsCTT	ENSP00000361423.2:n.964+274_964+276delinsCTT
NM_005157.5:c.907+274_907+276delinsCTT	NP_005148.2:n.907+274_907+276delinsCTT
NM_007313.2:c.964+274_964+276delinsCTT	NP_009297.2:n.964+274_964+276delinsCTT
NM_005157.6:c.907+274_907+276delinsCTT MANE Select	NP_005148.2:n.907+274_907+276delinsCTT
NM_007313.3:c.964+274_964+276delinsCTT	NP_009297.2:n.964+274_964+276delinsCTT