Canonical Allele Identifier: CA467394957

Gene: ABL1

Linked Data

• MyVariant Identifiers: chr9:g.133747524C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872137C>G , CM000671.2:g.130872137C>G	GRCh38
NC_000009.11:g.133747524C>G , CM000671.1:g.133747524C>G	GRCh37
NC_000009.10:g.132737345C>G	NCBI36
NG_012034.1:g.163257C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.888C>G	ENSP00000361423.2:p.Thr296=
ENST00000318560.6:c.831C>G MANE Select	ENSP00000323315.5:p.Thr277=
ENST00000372348.7:c.888C>G	ENSP00000361423.2:p.Thr296=
ENST00000318560.5:c.831C>G	ENSP00000323315.5:p.Thr277=
ENST00000372348.6:c.888C>G	ENSP00000361423.2:p.Thr296=
NM_005157.5:c.831C>G	NP_005148.2:p.Thr277=
NM_007313.2:c.888C>G	NP_009297.2:p.Thr296=
NM_005157.6:c.831C>G MANE Select	NP_005148.2:p.Thr277=
NM_007313.3:c.888C>G	NP_009297.2:p.Thr296=