Canonical Allele Identifier: CA2783315733
Gene: TEK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27172913_27172915del , CM000671.2:g.27172913_27172915del GRCh38
NC_000009.11:g.27172911_27172913del , CM000671.1:g.27172911_27172913del GRCh37
NC_000009.10:g.27162911_27162913del NCBI36
NG_011828.1:g.68765_68767del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380036.10:c.760+166_760+168del MANE Select ENSP00000369375.4:n.760+166_760+168del
ENST00000380036.8:c.760+166_760+168del ENSP00000369375.4:n.760+166_760+168del
ENST00000406359.8:c.760+166_760+168del ENSP00000383977.4:n.760+166_760+168del
ENST00000519080.1:c.319+166_319+168del ENSP00000428337.1:n.319+166_319+168del
ENST00000519097.5:c.448+166_448+168del ENSP00000430686.1:n.448+166_448+168del
ENST00000615002.4:c.760+166_760+168del ENSP00000480251.1:n.760+166_760+168del
NM_000459.4:c.760+166_760+168del NP_000450.2:n.760+166_760+168del
NM_001290077.1:c.760+166_760+168del NP_001277006.1:n.760+166_760+168del
NM_001290078.1:c.448+166_448+168del NP_001277007.1:n.448+166_448+168del
XM_005251561.1:c.760+166_760+168del XP_005251618.1:n.760+166_760+168del
XM_005251563.1:c.760+166_760+168del XP_005251620.1:n.760+166_760+168del
XM_005251561.2:c.760+166_760+168del XP_005251618.1:n.760+166_760+168del
XM_005251563.2:c.760+166_760+168del XP_005251620.1:n.760+166_760+168del
NM_000459.5:c.760+166_760+168del MANE Select NP_000450.3:n.760+166_760+168del
NM_001375475.1:c.760+166_760+168del NP_001362404.1:n.760+166_760+168del
NM_001375476.1:c.760+166_760+168del NP_001362405.1:n.760+166_760+168del