Canonical Allele Identifier: CA435815587

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133485138A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766294A>G , CM000665.2:g.133766294A>G	GRCh38
NC_000003.11:g.133485138A>G , CM000665.1:g.133485138A>G	GRCh37
NC_000003.10:g.134967828A>G	NCBI36
NG_013080.1:g.25162A>G
NG_013080.2:g.109297A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1347A>G MANE Select	ENSP00000385834.3:p.Ala449=
ENST00000402696.7:c.1347A>G	ENSP00000385834.3:p.Ala449=
ENST00000461695.1:c.17A>G
NM_001063.3:c.1347A>G	NP_001054.1:p.Ala449=
XM_011513100.1:c.1347A>G	XP_011511402.1:p.Ala449=
NM_001354703.1:c.1215A>G	NP_001341632.1:p.Ala405=
NM_001354704.1:c.966A>G	NP_001341633.1:p.Ala322=
NM_001063.4:c.1347A>G MANE Select	NP_001054.2:p.Ala449=
NM_001354703.2:c.1215A>G	NP_001341632.2:p.Ala405=
NM_001354704.2:c.966A>G	NP_001341633.2:p.Ala322=