Canonical Allele Identifier: CA435815813

Gene: TF

Linked Data

• COSMIC: COSM4973537
• MyVariant Identifiers: chr3:g.133494308G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775464G>C , CM000665.2:g.133775464G>C	GRCh38
NC_000003.11:g.133494308G>C , CM000665.1:g.133494308G>C	GRCh37
NC_000003.10:g.134976998G>C	NCBI36
NG_013080.1:g.34332G>C
NG_013080.2:g.118467G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1719G>C MANE Select	ENSP00000385834.3:p.Leu573=
ENST00000402696.7:c.1719G>C	ENSP00000385834.3:p.Leu573=
ENST00000461695.1:c.450G>C
ENST00000467842.1:n.2713G>C
NM_001063.3:c.1719G>C	NP_001054.1:p.Leu573=
XM_011513100.1:c.1719G>C	XP_011511402.1:p.Leu573=
NM_001354703.1:c.1587G>C	NP_001341632.1:p.Leu529=
NM_001354704.1:c.1338G>C	NP_001341633.1:p.Leu446=
NM_001063.4:c.1719G>C MANE Select	NP_001054.2:p.Leu573=
NM_001354703.2:c.1587G>C	NP_001341632.2:p.Leu529=
NM_001354704.2:c.1338G>C	NP_001341633.2:p.Leu446=