Canonical Allele Identifier: CA467496269

Gene: ABL1

Linked Data

• MyVariant Identifiers: chr9:g.133738272T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130862885T>A , CM000671.2:g.130862885T>A	GRCh38
NC_000009.11:g.133738272T>A , CM000671.1:g.133738272T>A	GRCh37
NC_000009.10:g.132728093T>A	NCBI36
NG_012034.1:g.154005T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.729T>A	ENSP00000361423.2:p.Thr243=
ENST00000318560.6:c.672T>A MANE Select	ENSP00000323315.5:p.Thr224=
ENST00000372348.7:c.729T>A	ENSP00000361423.2:p.Thr243=
ENST00000318560.5:c.672T>A	ENSP00000323315.5:p.Thr224=
ENST00000372348.6:c.729T>A	ENSP00000361423.2:p.Thr243=
NM_005157.5:c.672T>A	NP_005148.2:p.Thr224=
NM_007313.2:c.729T>A	NP_009297.2:p.Thr243=
NM_005157.6:c.672T>A MANE Select	NP_005148.2:p.Thr224=
NM_007313.3:c.729T>A	NP_009297.2:p.Thr243=