Canonical Allele Identifier: CA2577907430
Gene: TF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133777144_133777147del , CM000665.2:g.133777144_133777147del GRCh38
NC_000003.11:g.133495988_133495991del , CM000665.1:g.133495988_133495991del GRCh37
NC_000003.10:g.134978678_134978681del NCBI36
NG_013080.1:g.36012_36015del
NG_013080.2:g.120147_120150del

Transcript Alleles

HGVS Amino-acid Change
ENST00000402696.9:c.1968_1971del MANE Select ENSP00000385834.3:p.Cys656TrpfsTer14
ENST00000402696.7:c.1968_1971del ENSP00000385834.3:p.Cys656TrpfsTer14
ENST00000461695.1:c.699_702del
ENST00000467842.1:n.2962_2965del
NM_001063.3:c.1968_1971del NP_001054.1:p.Cys656TrpfsTer14
XM_011513100.1:c.1968_1971del XP_011511402.1:p.Cys656TrpfsTer14
NM_001354703.1:c.1836_1839del NP_001341632.1:p.Cys612TrpfsTer14
NM_001354704.1:c.1587_1590del NP_001341633.1:p.Cys529TrpfsTer14
NM_001063.4:c.1968_1971del MANE Select NP_001054.2:p.Cys656TrpfsTer14
NM_001354703.2:c.1836_1839del NP_001341632.2:p.Cys612TrpfsTer14
NM_001354704.2:c.1587_1590del NP_001341633.2:p.Cys529TrpfsTer14