Canonical Allele Identifier: CA435806362

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475734C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756890C>A , CM000665.2:g.133756890C>A	GRCh38
NC_000003.11:g.133475734C>A , CM000665.1:g.133475734C>A	GRCh37
NC_000003.10:g.134958424C>A	NCBI36
NG_013080.1:g.15758C>A
NG_013080.2:g.99893C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.751C>A MANE Select	ENSP00000385834.3:p.Arg251=
ENST00000402696.7:c.751C>A	ENSP00000385834.3:p.Arg251=
ENST00000482271.5:c.370C>A	ENSP00000419338.1:p.Arg124=
ENST00000485977.1:c.158-42C>A	ENSP00000418716.1:n.158-42C>A
NM_001063.3:c.751C>A	NP_001054.1:p.Arg251=
XM_011513100.1:c.751C>A	XP_011511402.1:p.Arg251=
NM_001354703.1:c.619C>A	NP_001341632.1:p.Arg207=
NM_001354704.1:c.370C>A	NP_001341633.1:p.Arg124=
NM_001063.4:c.751C>A MANE Select	NP_001054.2:p.Arg251=
NM_001354703.2:c.619C>A	NP_001341632.2:p.Arg207=
NM_001354704.2:c.370C>A	NP_001341633.2:p.Arg124=