Canonical Allele Identifier: CA354604957

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475809G>A (hg19) ; chr3:g.133756965G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756965G>A , CM000665.2:g.133756965G>A	GRCh38
NC_000003.11:g.133475809G>A , CM000665.1:g.133475809G>A	GRCh37
NC_000003.10:g.134958499G>A	NCBI36
NG_013080.1:g.15833G>A
NG_013080.2:g.99968G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.826G>A MANE Select	ENSP00000385834.3:p.Gly276Ser
ENST00000402696.7:c.826G>A	ENSP00000385834.3:p.Gly276Ser
ENST00000485977.1:c.191G>A	ENSP00000418716.1:p.Gly64Glu
NM_001063.3:c.826G>A	NP_001054.1:p.Gly276Ser
XM_011513100.1:c.826G>A	XP_011511402.1:p.Gly276Ser
NM_001354703.1:c.694G>A	NP_001341632.1:p.Gly232Ser
NM_001354704.1:c.445G>A	NP_001341633.1:p.Gly149Ser
NM_001063.4:c.826G>A MANE Select	NP_001054.2:p.Gly276Ser
NM_001354703.2:c.694G>A	NP_001341632.2:p.Gly232Ser
NM_001354704.2:c.445G>A	NP_001341633.2:p.Gly149Ser