Canonical Allele Identifier: CA435815646

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133485225C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766381C>A , CM000665.2:g.133766381C>A	GRCh38
NC_000003.11:g.133485225C>A , CM000665.1:g.133485225C>A	GRCh37
NC_000003.10:g.134967915C>A	NCBI36
NG_013080.1:g.25249C>A
NG_013080.2:g.109384C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1434C>A MANE Select	ENSP00000385834.3:p.Gly478=
ENST00000402696.7:c.1434C>A	ENSP00000385834.3:p.Gly478=
ENST00000461695.1:c.104C>A
NM_001063.3:c.1434C>A	NP_001054.1:p.Gly478=
XM_011513100.1:c.1434C>A	XP_011511402.1:p.Gly478=
NM_001354703.1:c.1302C>A	NP_001341632.1:p.Gly434=
NM_001354704.1:c.1053C>A	NP_001341633.1:p.Gly351=
NM_001063.4:c.1434C>A MANE Select	NP_001054.2:p.Gly478=
NM_001354703.2:c.1302C>A	NP_001341632.2:p.Gly434=
NM_001354704.2:c.1053C>A	NP_001341633.2:p.Gly351=