Canonical Allele Identifier: CA2783322681
Gene: TEK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27173468_27173469insGAT , CM000671.2:g.27173468_27173469insGAT GRCh38
NC_000009.11:g.27173466_27173467insGAT , CM000671.1:g.27173466_27173467insGAT GRCh37
NC_000009.10:g.27163466_27163467insGAT NCBI36
NG_011828.1:g.69320_69321insGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000380036.10:c.901+106_901+107insGAT MANE Select ENSP00000369375.4:n.901+106_901+107insGAT
ENST00000380036.8:c.901+106_901+107insGAT ENSP00000369375.4:n.901+106_901+107insGAT
ENST00000406359.8:c.901+106_901+107insGAT ENSP00000383977.4:n.901+106_901+107insGAT
ENST00000519080.1:c.460+106_460+107insGAT ENSP00000428337.1:n.460+106_460+107insGAT
ENST00000519097.5:c.589+106_589+107insGAT ENSP00000430686.1:n.589+106_589+107insGAT
ENST00000615002.4:c.901+106_901+107insGAT ENSP00000480251.1:n.901+106_901+107insGAT
NM_000459.4:c.901+106_901+107insGAT NP_000450.2:n.901+106_901+107insGAT
NM_001290077.1:c.901+106_901+107insGAT NP_001277006.1:n.901+106_901+107insGAT
NM_001290078.1:c.589+106_589+107insGAT NP_001277007.1:n.589+106_589+107insGAT
XM_005251561.1:c.901+106_901+107insGAT XP_005251618.1:n.901+106_901+107insGAT
XM_005251563.1:c.901+106_901+107insGAT XP_005251620.1:n.901+106_901+107insGAT
XM_005251561.2:c.901+106_901+107insGAT XP_005251618.1:n.901+106_901+107insGAT
XM_005251563.2:c.901+106_901+107insGAT XP_005251620.1:n.901+106_901+107insGAT
NM_000459.5:c.901+106_901+107insGAT MANE Select NP_000450.3:n.901+106_901+107insGAT
NM_001375475.1:c.901+106_901+107insGAT NP_001362404.1:n.901+106_901+107insGAT
NM_001375476.1:c.901+106_901+107insGAT NP_001362405.1:n.901+106_901+107insGAT