Canonical Allele Identifier: CA435806394

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475742G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756898G>C , CM000665.2:g.133756898G>C	GRCh38
NC_000003.11:g.133475742G>C , CM000665.1:g.133475742G>C	GRCh37
NC_000003.10:g.134958432G>C	NCBI36
NG_013080.1:g.15766G>C
NG_013080.2:g.99901G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.759G>C MANE Select	ENSP00000385834.3:p.Pro253=
ENST00000402696.7:c.759G>C	ENSP00000385834.3:p.Pro253=
ENST00000482271.5:c.378G>C	ENSP00000419338.1:p.Pro126=
ENST00000485977.1:c.158-34G>C	ENSP00000418716.1:n.158-34G>C
NM_001063.3:c.759G>C	NP_001054.1:p.Pro253=
XM_011513100.1:c.759G>C	XP_011511402.1:p.Pro253=
NM_001354703.1:c.627G>C	NP_001341632.1:p.Pro209=
NM_001354704.1:c.378G>C	NP_001341633.1:p.Pro126=
NM_001063.4:c.759G>C MANE Select	NP_001054.2:p.Pro253=
NM_001354703.2:c.627G>C	NP_001341632.2:p.Pro209=
NM_001354704.2:c.378G>C	NP_001341633.2:p.Pro126=