Canonical Allele Identifier: CA918434180
Gene: TEK HGNC NCBI

Linked Data

dbSNP Id: rs1564096313

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27204833_27204834del , CM000671.2:g.27204833_27204834del GRCh38
NC_000009.11:g.27204831_27204832del , CM000671.1:g.27204831_27204832del GRCh37
NC_000009.10:g.27194831_27194832del NCBI36
NG_011828.1:g.100685_100686del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380036.10:c.2210-78_2210-77del MANE Select ENSP00000369375.4:n.2210-78_2210-77del
ENST00000380036.8:c.2210-78_2210-77del ENSP00000369375.4:n.2210-78_2210-77del
ENST00000406359.8:c.2081-78_2081-77del ENSP00000383977.4:n.2081-78_2081-77del
ENST00000519097.5:c.1769-78_1769-77del ENSP00000430686.1:n.1769-78_1769-77del
ENST00000615002.4:c.*711-78_*711-77del ENSP00000480251.1:n.*711-78_*711-77del
NM_000459.4:c.2210-78_2210-77del NP_000450.2:n.2210-78_2210-77del
NM_001290077.1:c.2081-78_2081-77del NP_001277006.1:n.2081-78_2081-77del
NM_001290078.1:c.1769-78_1769-77del NP_001277007.1:n.1769-78_1769-77del
XM_005251561.1:c.2210-78_2210-77del XP_005251618.1:n.2210-78_2210-77del
XM_005251563.1:c.2081-78_2081-77del XP_005251620.1:n.2081-78_2081-77del
XM_005251561.2:c.2210-78_2210-77del XP_005251618.1:n.2210-78_2210-77del
XM_005251563.2:c.2081-78_2081-77del XP_005251620.1:n.2081-78_2081-77del
NM_000459.5:c.2210-78_2210-77del MANE Select NP_000450.3:n.2210-78_2210-77del
NM_001375475.1:c.2210-78_2210-77del NP_001362404.1:n.2210-78_2210-77del
NM_001375476.1:c.2081-78_2081-77del NP_001362405.1:n.2081-78_2081-77del