Canonical Allele Identifier: CA354604897

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475777T>G (hg19) ; chr3:g.133756933T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756933T>G , CM000665.2:g.133756933T>G	GRCh38
NC_000003.11:g.133475777T>G , CM000665.1:g.133475777T>G	GRCh37
NC_000003.10:g.134958467T>G	NCBI36
NG_013080.1:g.15801T>G
NG_013080.2:g.99936T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.794T>G MANE Select	ENSP00000385834.3:p.Val265Gly
ENST00000402696.7:c.794T>G	ENSP00000385834.3:p.Val265Gly
ENST00000485977.1:c.159T>G	ENSP00000418716.1:p.Gly53=
NM_001063.3:c.794T>G	NP_001054.1:p.Val265Gly
XM_011513100.1:c.794T>G	XP_011511402.1:p.Val265Gly
NM_001354703.1:c.662T>G	NP_001341632.1:p.Val221Gly
NM_001354704.1:c.413T>G	NP_001341633.1:p.Val138Gly
NM_001063.4:c.794T>G MANE Select	NP_001054.2:p.Val265Gly
NM_001354703.2:c.662T>G	NP_001341632.2:p.Val221Gly
NM_001354704.2:c.413T>G	NP_001341633.2:p.Val138Gly