Canonical Allele Identifier: CA354604979

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475820G>C (hg19) ; chr3:g.133756976G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756976G>C , CM000665.2:g.133756976G>C	GRCh38
NC_000003.11:g.133475820G>C , CM000665.1:g.133475820G>C	GRCh37
NC_000003.10:g.134958510G>C	NCBI36
NG_013080.1:g.15844G>C
NG_013080.2:g.99979G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.837G>C MANE Select	ENSP00000385834.3:p.Glu279Asp
ENST00000402696.7:c.837G>C	ENSP00000385834.3:p.Glu279Asp
ENST00000485977.1:c.202G>C	ENSP00000418716.1:p.Gly68Arg
NM_001063.3:c.837G>C	NP_001054.1:p.Glu279Asp
XM_011513100.1:c.837G>C	XP_011511402.1:p.Glu279Asp
NM_001354703.1:c.705G>C	NP_001341632.1:p.Glu235Asp
NM_001354704.1:c.456G>C	NP_001341633.1:p.Glu152Asp
NM_001063.4:c.837G>C MANE Select	NP_001054.2:p.Glu279Asp
NM_001354703.2:c.705G>C	NP_001341632.2:p.Glu235Asp
NM_001354704.2:c.456G>C	NP_001341633.2:p.Glu152Asp