Canonical Allele Identifier: CA354604963

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475813G>C (hg19) ; chr3:g.133756969G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756969G>C , CM000665.2:g.133756969G>C	GRCh38
NC_000003.11:g.133475813G>C , CM000665.1:g.133475813G>C	GRCh37
NC_000003.10:g.134958503G>C	NCBI36
NG_013080.1:g.15837G>C
NG_013080.2:g.99972G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.830G>C MANE Select	ENSP00000385834.3:p.Gly277Ala
ENST00000402696.7:c.830G>C	ENSP00000385834.3:p.Gly277Ala
ENST00000485977.1:c.195G>C	ENSP00000418716.1:p.Arg65=
NM_001063.3:c.830G>C	NP_001054.1:p.Gly277Ala
XM_011513100.1:c.830G>C	XP_011511402.1:p.Gly277Ala
NM_001354703.1:c.698G>C	NP_001341632.1:p.Gly233Ala
NM_001354704.1:c.449G>C	NP_001341633.1:p.Gly150Ala
NM_001063.4:c.830G>C MANE Select	NP_001054.2:p.Gly277Ala
NM_001354703.2:c.698G>C	NP_001341632.2:p.Gly233Ala
NM_001354704.2:c.449G>C	NP_001341633.2:p.Gly150Ala