Canonical Allele Identifier: CA2689641554
Gene: TEK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27173514_27173515insTGATTC , CM000671.2:g.27173514_27173515insTGATTC GRCh38
NC_000009.11:g.27173512_27173513insTGATTC , CM000671.1:g.27173512_27173513insTGATTC GRCh37
NC_000009.10:g.27163512_27163513insTGATTC NCBI36
NG_011828.1:g.69366_69367insTGATTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000380036.10:c.901+152_901+153insTGATTC MANE Select ENSP00000369375.4:n.901+152_901+153insTGATTC
ENST00000380036.8:c.901+152_901+153insTGATTC ENSP00000369375.4:n.901+152_901+153insTGATTC
ENST00000406359.8:c.901+152_901+153insTGATTC ENSP00000383977.4:n.901+152_901+153insTGATTC
ENST00000519080.1:c.460+152_460+153insTGATTC ENSP00000428337.1:n.460+152_460+153insTGATTC
ENST00000519097.5:c.589+152_589+153insTGATTC ENSP00000430686.1:n.589+152_589+153insTGATTC
ENST00000615002.4:c.901+152_901+153insTGATTC ENSP00000480251.1:n.901+152_901+153insTGATTC
NM_000459.4:c.901+152_901+153insTGATTC NP_000450.2:n.901+152_901+153insTGATTC
NM_001290077.1:c.901+152_901+153insTGATTC NP_001277006.1:n.901+152_901+153insTGATTC
NM_001290078.1:c.589+152_589+153insTGATTC NP_001277007.1:n.589+152_589+153insTGATTC
XM_005251561.1:c.901+152_901+153insTGATTC XP_005251618.1:n.901+152_901+153insTGATTC
XM_005251563.1:c.901+152_901+153insTGATTC XP_005251620.1:n.901+152_901+153insTGATTC
XM_005251561.2:c.901+152_901+153insTGATTC XP_005251618.1:n.901+152_901+153insTGATTC
XM_005251563.2:c.901+152_901+153insTGATTC XP_005251620.1:n.901+152_901+153insTGATTC
NM_000459.5:c.901+152_901+153insTGATTC MANE Select NP_000450.3:n.901+152_901+153insTGATTC
NM_001375475.1:c.901+152_901+153insTGATTC NP_001362404.1:n.901+152_901+153insTGATTC
NM_001375476.1:c.901+152_901+153insTGATTC NP_001362405.1:n.901+152_901+153insTGATTC