Canonical Allele Identifier: CA2783322697
Gene: TEK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27173492_27173493insA , CM000671.2:g.27173492_27173493insA GRCh38
NC_000009.11:g.27173490_27173491insA , CM000671.1:g.27173490_27173491insA GRCh37
NC_000009.10:g.27163490_27163491insA NCBI36
NG_011828.1:g.69344_69345insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000380036.10:c.901+130_901+131insA MANE Select ENSP00000369375.4:n.901+130_901+131insA
ENST00000380036.8:c.901+130_901+131insA ENSP00000369375.4:n.901+130_901+131insA
ENST00000406359.8:c.901+130_901+131insA ENSP00000383977.4:n.901+130_901+131insA
ENST00000519080.1:c.460+130_460+131insA ENSP00000428337.1:n.460+130_460+131insA
ENST00000519097.5:c.589+130_589+131insA ENSP00000430686.1:n.589+130_589+131insA
ENST00000615002.4:c.901+130_901+131insA ENSP00000480251.1:n.901+130_901+131insA
NM_000459.4:c.901+130_901+131insA NP_000450.2:n.901+130_901+131insA
NM_001290077.1:c.901+130_901+131insA NP_001277006.1:n.901+130_901+131insA
NM_001290078.1:c.589+130_589+131insA NP_001277007.1:n.589+130_589+131insA
XM_005251561.1:c.901+130_901+131insA XP_005251618.1:n.901+130_901+131insA
XM_005251563.1:c.901+130_901+131insA XP_005251620.1:n.901+130_901+131insA
XM_005251561.2:c.901+130_901+131insA XP_005251618.1:n.901+130_901+131insA
XM_005251563.2:c.901+130_901+131insA XP_005251620.1:n.901+130_901+131insA
NM_000459.5:c.901+130_901+131insA MANE Select NP_000450.3:n.901+130_901+131insA
NM_001375475.1:c.901+130_901+131insA NP_001362404.1:n.901+130_901+131insA
NM_001375476.1:c.901+130_901+131insA NP_001362405.1:n.901+130_901+131insA