Canonical Allele Identifier: CA354604848

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475756A>G (hg19) ; chr3:g.133756912A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756912A>G , CM000665.2:g.133756912A>G	GRCh38
NC_000003.11:g.133475756A>G , CM000665.1:g.133475756A>G	GRCh37
NC_000003.10:g.134958446A>G	NCBI36
NG_013080.1:g.15780A>G
NG_013080.2:g.99915A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.773A>G MANE Select	ENSP00000385834.3:p.Lys258Arg
ENST00000402696.7:c.773A>G	ENSP00000385834.3:p.Lys258Arg
ENST00000482271.5:c.392A>G	ENSP00000419338.1:p.Lys131Arg
ENST00000485977.1:c.158-20A>G	ENSP00000418716.1:n.158-20A>G
NM_001063.3:c.773A>G	NP_001054.1:p.Lys258Arg
XM_011513100.1:c.773A>G	XP_011511402.1:p.Lys258Arg
NM_001354703.1:c.641A>G	NP_001341632.1:p.Lys214Arg
NM_001354704.1:c.392A>G	NP_001341633.1:p.Lys131Arg
NM_001063.4:c.773A>G MANE Select	NP_001054.2:p.Lys258Arg
NM_001354703.2:c.641A>G	NP_001341632.2:p.Lys214Arg
NM_001354704.2:c.392A>G	NP_001341633.2:p.Lys131Arg