Canonical Allele Identifier: CA435806682

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475824T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756980T>C , CM000665.2:g.133756980T>C	GRCh38
NC_000003.11:g.133475824T>C , CM000665.1:g.133475824T>C	GRCh37
NC_000003.10:g.134958514T>C	NCBI36
NG_013080.1:g.15848T>C
NG_013080.2:g.99983T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.841T>C MANE Select	ENSP00000385834.3:p.Leu281=
ENST00000402696.7:c.841T>C	ENSP00000385834.3:p.Leu281=
ENST00000485977.1:c.206T>C	ENSP00000418716.1:p.Leu69Pro
NM_001063.3:c.841T>C	NP_001054.1:p.Leu281=
XM_011513100.1:c.841T>C	XP_011511402.1:p.Leu281=
NM_001354703.1:c.709T>C	NP_001341632.1:p.Leu237=
NM_001354704.1:c.460T>C	NP_001341633.1:p.Leu154=
NM_001063.4:c.841T>C MANE Select	NP_001054.2:p.Leu281=
NM_001354703.2:c.709T>C	NP_001341632.2:p.Leu237=
NM_001354704.2:c.460T>C	NP_001341633.2:p.Leu154=