Canonical Allele Identifier: CA467395212

Gene: ABL1

Linked Data

• MyVariant Identifiers: chr9:g.133748413C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130873026C>T , CM000671.2:g.130873026C>T	GRCh38
NC_000009.11:g.133748413C>T , CM000671.1:g.133748413C>T	GRCh37
NC_000009.10:g.132738234C>T	NCBI36
NG_012034.1:g.164146C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000372348.9:c.1131C>T	ENSP00000361423.2:p.Asn377=
ENST00000318560.6:c.1074C>T MANE Select	ENSP00000323315.5:p.Asn358=
ENST00000372348.7:c.1131C>T	ENSP00000361423.2:p.Asn377=
ENST00000318560.5:c.1074C>T	ENSP00000323315.5:p.Asn358=
ENST00000372348.6:c.1131C>T	ENSP00000361423.2:p.Asn377=
NM_005157.5:c.1074C>T	NP_005148.2:p.Asn358=
NM_007313.2:c.1131C>T	NP_009297.2:p.Asn377=
NM_005157.6:c.1074C>T MANE Select	NP_005148.2:p.Asn358=
NM_007313.3:c.1131C>T	NP_009297.2:p.Asn377=