Canonical Allele Identifier: CA354604771

Gene: TF

Linked Data

• COSMIC: COSM1038562
• MyVariant Identifiers: chr3:g.133475720G>A (hg19) ; chr3:g.133756876G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756876G>A , CM000665.2:g.133756876G>A	GRCh38
NC_000003.11:g.133475720G>A , CM000665.1:g.133475720G>A	GRCh37
NC_000003.10:g.134958410G>A	NCBI36
NG_013080.1:g.15744G>A
NG_013080.2:g.99879G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.737G>A MANE Select	ENSP00000385834.3:p.Cys246Tyr
ENST00000402696.7:c.737G>A	ENSP00000385834.3:p.Cys246Tyr
ENST00000482271.5:c.356G>A	ENSP00000419338.1:p.Cys119Tyr
ENST00000485977.1:c.158-56G>A	ENSP00000418716.1:n.158-56G>A
NM_001063.3:c.737G>A	NP_001054.1:p.Cys246Tyr
XM_011513100.1:c.737G>A	XP_011511402.1:p.Cys246Tyr
NM_001354703.1:c.605G>A	NP_001341632.1:p.Cys202Tyr
NM_001354704.1:c.356G>A	NP_001341633.1:p.Cys119Tyr
NM_001063.4:c.737G>A MANE Select	NP_001054.2:p.Cys246Tyr
NM_001354703.2:c.605G>A	NP_001341632.2:p.Cys202Tyr
NM_001354704.2:c.356G>A	NP_001341633.2:p.Cys119Tyr