Canonical Allele Identifier: CA354605006

Gene: TF

Linked Data

• gnomAD v4: 3-133756988-G-A
• MyVariant Identifiers: chr3:g.133475832G>A (hg19) ; chr3:g.133756988G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756988G>A , CM000665.2:g.133756988G>A	GRCh38
NC_000003.11:g.133475832G>A , CM000665.1:g.133475832G>A	GRCh37
NC_000003.10:g.134958522G>A	NCBI36
NG_013080.1:g.15856G>A
NG_013080.2:g.99991G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.849G>A MANE Select	ENSP00000385834.3:p.Trp283Ter
ENST00000402696.7:c.849G>A	ENSP00000385834.3:p.Trp283Ter
ENST00000485977.1:c.214G>A	ENSP00000418716.1:p.Gly72Arg
NM_001063.3:c.849G>A	NP_001054.1:p.Trp283Ter
XM_011513100.1:c.849G>A	XP_011511402.1:p.Trp283Ter
NM_001354703.1:c.717G>A	NP_001341632.1:p.Trp239Ter
NM_001354704.1:c.468G>A	NP_001341633.1:p.Trp156Ter
NM_001063.4:c.849G>A MANE Select	NP_001054.2:p.Trp283Ter
NM_001354703.2:c.717G>A	NP_001341632.2:p.Trp239Ter
NM_001354704.2:c.468G>A	NP_001341633.2:p.Trp156Ter