Canonical Allele Identifier: CA2580079801

Gene: ABL1

Linked Data

• ClinVar Variation Id: 2438792
• ClinVar RCV Id: RCV003139544

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872132del , CM000671.2:g.130872132del	GRCh38
NC_000009.11:g.133747519del , CM000671.1:g.133747519del	GRCh37
NC_000009.10:g.132737340del	NCBI36
NG_012034.1:g.163252del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.883del	ENSP00000361423.2:p.Asp295ThrfsTer9
ENST00000318560.6:c.826del MANE Select	ENSP00000323315.5:p.Asp276ThrfsTer9
ENST00000372348.7:c.883del	ENSP00000361423.2:p.Asp295ThrfsTer9
ENST00000318560.5:c.826del	ENSP00000323315.5:p.Asp276ThrfsTer9
ENST00000372348.6:c.883del	ENSP00000361423.2:p.Asp295ThrfsTer9
NM_005157.5:c.826del	NP_005148.2:p.Asp276ThrfsTer9
NM_007313.2:c.883del	NP_009297.2:p.Asp295ThrfsTer9
NM_005157.6:c.826del MANE Select	NP_005148.2:p.Asp276ThrfsTer9
NM_007313.3:c.883del	NP_009297.2:p.Asp295ThrfsTer9