Canonical Allele Identifier: CA354604857

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475759A>T (hg19) ; chr3:g.133756915A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756915A>T , CM000665.2:g.133756915A>T	GRCh38
NC_000003.11:g.133475759A>T , CM000665.1:g.133475759A>T	GRCh37
NC_000003.10:g.134958449A>T	NCBI36
NG_013080.1:g.15783A>T
NG_013080.2:g.99918A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.776A>T MANE Select	ENSP00000385834.3:p.Asp259Val
ENST00000402696.7:c.776A>T	ENSP00000385834.3:p.Asp259Val
ENST00000482271.5:c.395A>T	ENSP00000419338.1:p.Asp132Val
ENST00000485977.1:c.158-17A>T	ENSP00000418716.1:n.158-17A>T
NM_001063.3:c.776A>T	NP_001054.1:p.Asp259Val
XM_011513100.1:c.776A>T	XP_011511402.1:p.Asp259Val
NM_001354703.1:c.644A>T	NP_001341632.1:p.Asp215Val
NM_001354704.1:c.395A>T	NP_001341633.1:p.Asp132Val
NM_001063.4:c.776A>T MANE Select	NP_001054.2:p.Asp259Val
NM_001354703.2:c.644A>T	NP_001341632.2:p.Asp215Val
NM_001354704.2:c.395A>T	NP_001341633.2:p.Asp132Val