Canonical Allele Identifier: CA354604984

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475822A>C (hg19) ; chr3:g.133756978A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756978A>C , CM000665.2:g.133756978A>C	GRCh38
NC_000003.11:g.133475822A>C , CM000665.1:g.133475822A>C	GRCh37
NC_000003.10:g.134958512A>C	NCBI36
NG_013080.1:g.15846A>C
NG_013080.2:g.99981A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.839A>C MANE Select	ENSP00000385834.3:p.Asp280Ala
ENST00000402696.7:c.839A>C	ENSP00000385834.3:p.Asp280Ala
ENST00000485977.1:c.204A>C	ENSP00000418716.1:p.Gly68=
NM_001063.3:c.839A>C	NP_001054.1:p.Asp280Ala
XM_011513100.1:c.839A>C	XP_011511402.1:p.Asp280Ala
NM_001354703.1:c.707A>C	NP_001341632.1:p.Asp236Ala
NM_001354704.1:c.458A>C	NP_001341633.1:p.Asp153Ala
NM_001063.4:c.839A>C MANE Select	NP_001054.2:p.Asp280Ala
NM_001354703.2:c.707A>C	NP_001341632.2:p.Asp236Ala
NM_001354704.2:c.458A>C	NP_001341633.2:p.Asp153Ala