Canonical Allele Identifier: CA435815944

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133495991G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777147G>A , CM000665.2:g.133777147G>A	GRCh38
NC_000003.11:g.133495991G>A , CM000665.1:g.133495991G>A	GRCh37
NC_000003.10:g.134978681G>A	NCBI36
NG_013080.1:g.36015G>A
NG_013080.2:g.120150G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1971G>A MANE Select	ENSP00000385834.3:p.Leu657=
ENST00000402696.7:c.1971G>A	ENSP00000385834.3:p.Leu657=
ENST00000461695.1:c.702G>A
ENST00000467842.1:n.2965G>A
NM_001063.3:c.1971G>A	NP_001054.1:p.Leu657=
XM_011513100.1:c.1971G>A	XP_011511402.1:p.Leu657=
NM_001354703.1:c.1839G>A	NP_001341632.1:p.Leu613=
NM_001354704.1:c.1590G>A	NP_001341633.1:p.Leu530=
NM_001063.4:c.1971G>A MANE Select	NP_001054.2:p.Leu657=
NM_001354703.2:c.1839G>A	NP_001341632.2:p.Leu613=
NM_001354704.2:c.1590G>A	NP_001341633.2:p.Leu530=