Canonical Allele Identifier: CA354610380

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133494365G>C (hg19) ; chr3:g.133775521G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775521G>C , CM000665.2:g.133775521G>C	GRCh38
NC_000003.11:g.133494365G>C , CM000665.1:g.133494365G>C	GRCh37
NC_000003.10:g.134977055G>C	NCBI36
NG_013080.1:g.34389G>C
NG_013080.2:g.118524G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1776G>C MANE Select	ENSP00000385834.3:p.Glu592Asp
ENST00000402696.7:c.1776G>C	ENSP00000385834.3:p.Glu592Asp
ENST00000461695.1:c.507G>C
ENST00000467842.1:n.2770G>C
NM_001063.3:c.1776G>C	NP_001054.1:p.Glu592Asp
XM_011513100.1:c.1776G>C	XP_011511402.1:p.Glu592Asp
NM_001354703.1:c.1644G>C	NP_001341632.1:p.Glu548Asp
NM_001354704.1:c.1395G>C	NP_001341633.1:p.Glu465Asp
NM_001063.4:c.1776G>C MANE Select	NP_001054.2:p.Glu592Asp
NM_001354703.2:c.1644G>C	NP_001341632.2:p.Glu548Asp
NM_001354704.2:c.1395G>C	NP_001341633.2:p.Glu465Asp