Canonical Allele Identifier: CA645556982
Gene: ABL1 HGNC NCBI

Linked Data

COSMIC: COSM130411

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872895_130872896delinsCT , CM000671.2:g.130872895_130872896delinsCT GRCh38
NC_000009.11:g.133748282_133748283delinsCT , CM000671.1:g.133748282_133748283delinsCT GRCh37
NC_000009.10:g.132738103_132738104delinsCT NCBI36
NG_012034.1:g.164015_164016delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.1000_1001delinsCT ENSP00000361423.2:p.Thr334Leu
ENST00000318560.6:c.943_944delinsCT MANE Select ENSP00000323315.5:p.Thr315Leu
ENST00000372348.7:c.1000_1001delinsCT ENSP00000361423.2:p.Thr334Leu
ENST00000318560.5:c.943_944delinsCT ENSP00000323315.5:p.Thr315Leu
ENST00000372348.6:c.1000_1001delinsCT ENSP00000361423.2:p.Thr334Leu
NM_005157.5:c.943_944delinsCT NP_005148.2:p.Thr315Leu
NM_007313.2:c.1000_1001delinsCT NP_009297.2:p.Thr334Leu
NM_005157.6:c.943_944delinsCT MANE Select NP_005148.2:p.Thr315Leu
NM_007313.3:c.1000_1001delinsCT NP_009297.2:p.Thr334Leu