Canonical Allele Identifier: CA2689643893
Gene: TEK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27212697_27212700del , CM000671.2:g.27212697_27212700del GRCh38
NC_000009.11:g.27212695_27212698del , CM000671.1:g.27212695_27212698del GRCh37
NC_000009.10:g.27202695_27202698del NCBI36
NG_011828.1:g.108549_108552del

Transcript Alleles

HGVS Amino-acid change
ENST00000380036.10:c.2687-10_2687-7del MANE Select ENSP00000369375.4:n.2687-10_2687-7del
ENST00000380036.8:c.2687-10_2687-7del ENSP00000369375.4:n.2687-10_2687-7del
ENST00000406359.8:c.2558-10_2558-7del ENSP00000383977.4:n.2558-10_2558-7del
ENST00000519097.5:c.2243-10_2243-7del ENSP00000430686.1:n.2243-10_2243-7del
ENST00000615002.4:c.*1188-10_*1188-7del ENSP00000480251.1:n.*1188-10_*1188-7del
NM_000459.4:c.2687-10_2687-7del NP_000450.2:n.2687-10_2687-7del
NM_001290077.1:c.2558-10_2558-7del NP_001277006.1:n.2558-10_2558-7del
NM_001290078.1:c.2243-10_2243-7del NP_001277007.1:n.2243-10_2243-7del
XM_005251561.1:c.2684-10_2684-7del XP_005251618.1:n.2684-10_2684-7del
XM_005251563.1:c.2555-10_2555-7del XP_005251620.1:n.2555-10_2555-7del
XM_005251561.2:c.2684-10_2684-7del XP_005251618.1:n.2684-10_2684-7del
XM_005251563.2:c.2555-10_2555-7del XP_005251620.1:n.2555-10_2555-7del
NM_000459.5:c.2687-10_2687-7del MANE Select NP_000450.3:n.2687-10_2687-7del
NM_001375475.1:c.2684-10_2684-7del NP_001362404.1:n.2684-10_2684-7del
NM_001375476.1:c.2555-10_2555-7del NP_001362405.1:n.2555-10_2555-7del