Canonical Allele Identifier: CA354610123
Gene: TF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133775450T>A , CM000665.2:g.133775450T>A GRCh38
NC_000003.11:g.133494294T>A , CM000665.1:g.133494294T>A GRCh37
NC_000003.10:g.134976984T>A NCBI36
NG_013080.1:g.34318T>A
NG_013080.2:g.118453T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000402696.9:c.1705T>A MANE Select ENSP00000385834.3:p.Trp569Arg
ENST00000402696.7:c.1705T>A ENSP00000385834.3:p.Trp569Arg
ENST00000461695.1:c.436T>A
ENST00000467842.1:n.2699T>A
NM_001063.3:c.1705T>A NP_001054.1:p.Trp569Arg
XM_011513100.1:c.1705T>A XP_011511402.1:p.Trp569Arg
NM_001354703.1:c.1573T>A NP_001341632.1:p.Trp525Arg
NM_001354704.1:c.1324T>A NP_001341633.1:p.Trp442Arg
NM_001063.4:c.1705T>A MANE Select NP_001054.2:p.Trp569Arg
NM_001354703.2:c.1573T>A NP_001341632.2:p.Trp525Arg
NM_001354704.2:c.1324T>A NP_001341633.2:p.Trp442Arg