Canonical Allele Identifier: CA435806358

Gene: TF

Linked Data

• COSMIC: COSM5674430
• MyVariant Identifiers: chr3:g.133475733C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756889C>G , CM000665.2:g.133756889C>G	GRCh38
NC_000003.11:g.133475733C>G , CM000665.1:g.133475733C>G	GRCh37
NC_000003.10:g.134958423C>G	NCBI36
NG_013080.1:g.15757C>G
NG_013080.2:g.99892C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.750C>G MANE Select	ENSP00000385834.3:p.Thr250=
ENST00000402696.7:c.750C>G	ENSP00000385834.3:p.Thr250=
ENST00000482271.5:c.369C>G	ENSP00000419338.1:p.Thr123=
ENST00000485977.1:c.158-43C>G	ENSP00000418716.1:n.158-43C>G
NM_001063.3:c.750C>G	NP_001054.1:p.Thr250=
XM_011513100.1:c.750C>G	XP_011511402.1:p.Thr250=
NM_001354703.1:c.618C>G	NP_001341632.1:p.Thr206=
NM_001354704.1:c.369C>G	NP_001341633.1:p.Thr123=
NM_001063.4:c.750C>G MANE Select	NP_001054.2:p.Thr250=
NM_001354703.2:c.618C>G	NP_001341632.2:p.Thr206=
NM_001354704.2:c.369C>G	NP_001341633.2:p.Thr123=