Canonical Allele Identifier: CA435806700

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475853G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757009G>A , CM000665.2:g.133757009G>A	GRCh38
NC_000003.11:g.133475853G>A , CM000665.1:g.133475853G>A	GRCh37
NC_000003.10:g.134958543G>A	NCBI36
NG_013080.1:g.15877G>A
NG_013080.2:g.100012G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870G>A MANE Select	ENSP00000385834.3:p.Gln290=
ENST00000402696.7:c.870G>A	ENSP00000385834.3:p.Gln290=
ENST00000485977.1:c.235G>A	ENSP00000418716.1:p.Gly79Arg
NM_001063.3:c.870G>A	NP_001054.1:p.Gln290=
XM_011513100.1:c.870G>A	XP_011511402.1:p.Gln290=
NM_001354703.1:c.738G>A	NP_001341632.1:p.Gln246=
NM_001354704.1:c.489G>A	NP_001341633.1:p.Gln163=
NM_001063.4:c.870G>A MANE Select	NP_001054.2:p.Gln290=
NM_001354703.2:c.738G>A	NP_001341632.2:p.Gln246=
NM_001354704.2:c.489G>A	NP_001341633.2:p.Gln163=