Canonical Allele Identifier: CA354604959

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475810G>C (hg19) ; chr3:g.133756966G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756966G>C , CM000665.2:g.133756966G>C	GRCh38
NC_000003.11:g.133475810G>C , CM000665.1:g.133475810G>C	GRCh37
NC_000003.10:g.134958500G>C	NCBI36
NG_013080.1:g.15834G>C
NG_013080.2:g.99969G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.827G>C MANE Select	ENSP00000385834.3:p.Gly276Ala
ENST00000402696.7:c.827G>C	ENSP00000385834.3:p.Gly276Ala
ENST00000485977.1:c.192G>C	ENSP00000418716.1:p.Gly64=
NM_001063.3:c.827G>C	NP_001054.1:p.Gly276Ala
XM_011513100.1:c.827G>C	XP_011511402.1:p.Gly276Ala
NM_001354703.1:c.695G>C	NP_001341632.1:p.Gly232Ala
NM_001354704.1:c.446G>C	NP_001341633.1:p.Gly149Ala
NM_001063.4:c.827G>C MANE Select	NP_001054.2:p.Gly276Ala
NM_001354703.2:c.695G>C	NP_001341632.2:p.Gly232Ala
NM_001354704.2:c.446G>C	NP_001341633.2:p.Gly149Ala