Canonical Allele Identifier: CA2783322699
Gene: TEK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27173495_27173496insGT , CM000671.2:g.27173495_27173496insGT GRCh38
NC_000009.11:g.27173493_27173494insGT , CM000671.1:g.27173493_27173494insGT GRCh37
NC_000009.10:g.27163493_27163494insGT NCBI36
NG_011828.1:g.69347_69348insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000380036.10:c.901+133_901+134insGT MANE Select ENSP00000369375.4:n.901+133_901+134insGT
ENST00000380036.8:c.901+133_901+134insGT ENSP00000369375.4:n.901+133_901+134insGT
ENST00000406359.8:c.901+133_901+134insGT ENSP00000383977.4:n.901+133_901+134insGT
ENST00000519080.1:c.460+133_460+134insGT ENSP00000428337.1:n.460+133_460+134insGT
ENST00000519097.5:c.589+133_589+134insGT ENSP00000430686.1:n.589+133_589+134insGT
ENST00000615002.4:c.901+133_901+134insGT ENSP00000480251.1:n.901+133_901+134insGT
NM_000459.4:c.901+133_901+134insGT NP_000450.2:n.901+133_901+134insGT
NM_001290077.1:c.901+133_901+134insGT NP_001277006.1:n.901+133_901+134insGT
NM_001290078.1:c.589+133_589+134insGT NP_001277007.1:n.589+133_589+134insGT
XM_005251561.1:c.901+133_901+134insGT XP_005251618.1:n.901+133_901+134insGT
XM_005251563.1:c.901+133_901+134insGT XP_005251620.1:n.901+133_901+134insGT
XM_005251561.2:c.901+133_901+134insGT XP_005251618.1:n.901+133_901+134insGT
XM_005251563.2:c.901+133_901+134insGT XP_005251620.1:n.901+133_901+134insGT
NM_000459.5:c.901+133_901+134insGT MANE Select NP_000450.3:n.901+133_901+134insGT
NM_001375475.1:c.901+133_901+134insGT NP_001362404.1:n.901+133_901+134insGT
NM_001375476.1:c.901+133_901+134insGT NP_001362405.1:n.901+133_901+134insGT