Canonical Allele Identifier: CA354604931

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475797G>A (hg19) ; chr3:g.133756953G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756953G>A , CM000665.2:g.133756953G>A	GRCh38
NC_000003.11:g.133475797G>A , CM000665.1:g.133475797G>A	GRCh37
NC_000003.10:g.134958487G>A	NCBI36
NG_013080.1:g.15821G>A
NG_013080.2:g.99956G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.814G>A MANE Select	ENSP00000385834.3:p.Ala272Thr
ENST00000402696.7:c.814G>A	ENSP00000385834.3:p.Ala272Thr
ENST00000485977.1:c.179G>A	ENSP00000418716.1:p.Gly60Asp
NM_001063.3:c.814G>A	NP_001054.1:p.Ala272Thr
XM_011513100.1:c.814G>A	XP_011511402.1:p.Ala272Thr
NM_001354703.1:c.682G>A	NP_001341632.1:p.Ala228Thr
NM_001354704.1:c.433G>A	NP_001341633.1:p.Ala145Thr
NM_001063.4:c.814G>A MANE Select	NP_001054.2:p.Ala272Thr
NM_001354703.2:c.682G>A	NP_001341632.2:p.Ala228Thr
NM_001354704.2:c.433G>A	NP_001341633.2:p.Ala145Thr