Canonical Allele Identifier: CA354604901

Gene: TF

Linked Data

• COSMIC: COSM3587657
• MyVariant Identifiers: chr3:g.133475779C>T (hg19) ; chr3:g.133756935C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756935C>T , CM000665.2:g.133756935C>T	GRCh38
NC_000003.11:g.133475779C>T , CM000665.1:g.133475779C>T	GRCh37
NC_000003.10:g.134958469C>T	NCBI36
NG_013080.1:g.15803C>T
NG_013080.2:g.99938C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.796C>T MANE Select	ENSP00000385834.3:p.Pro266Ser
ENST00000402696.7:c.796C>T	ENSP00000385834.3:p.Pro266Ser
ENST00000485977.1:c.161C>T	ENSP00000418716.1:p.Pro54Leu
NM_001063.3:c.796C>T	NP_001054.1:p.Pro266Ser
XM_011513100.1:c.796C>T	XP_011511402.1:p.Pro266Ser
NM_001354703.1:c.664C>T	NP_001341632.1:p.Pro222Ser
NM_001354704.1:c.415C>T	NP_001341633.1:p.Pro139Ser
NM_001063.4:c.796C>T MANE Select	NP_001054.2:p.Pro266Ser
NM_001354703.2:c.664C>T	NP_001341632.2:p.Pro222Ser
NM_001354704.2:c.415C>T	NP_001341633.2:p.Pro139Ser