Canonical Allele Identifier: CA467395187

Gene: ABL1

Linked Data

• MyVariant Identifiers: chr9:g.133748386A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872999A>T , CM000671.2:g.130872999A>T	GRCh38
NC_000009.11:g.133748386A>T , CM000671.1:g.133748386A>T	GRCh37
NC_000009.10:g.132738207A>T	NCBI36
NG_012034.1:g.164119A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.1104A>T	ENSP00000361423.2:p.Ser368=
ENST00000318560.6:c.1047A>T MANE Select	ENSP00000323315.5:p.Ser349=
ENST00000372348.7:c.1104A>T	ENSP00000361423.2:p.Ser368=
ENST00000318560.5:c.1047A>T	ENSP00000323315.5:p.Ser349=
ENST00000372348.6:c.1104A>T	ENSP00000361423.2:p.Ser368=
NM_005157.5:c.1047A>T	NP_005148.2:p.Ser349=
NM_007313.2:c.1104A>T	NP_009297.2:p.Ser368=
NM_005157.6:c.1047A>T MANE Select	NP_005148.2:p.Ser349=
NM_007313.3:c.1104A>T	NP_009297.2:p.Ser368=