Canonical Allele Identifier: CA1842021846

Gene: TEK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27173381_27173382delinsCT , CM000671.2:g.27173381_27173382delinsCT	GRCh38
NC_000009.11:g.27173379_27173380delinsCT , CM000671.1:g.27173379_27173380delinsCT	GRCh37
NC_000009.10:g.27163379_27163380delinsCT	NCBI36
NG_011828.1:g.69233_69234delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.901+19_901+20delinsCT MANE Select	ENSP00000369375.4:n.901+19_901+20delinsCT
ENST00000380036.8:c.901+19_901+20delinsCT	ENSP00000369375.4:n.901+19_901+20delinsCT
ENST00000406359.8:c.901+19_901+20delinsCT	ENSP00000383977.4:n.901+19_901+20delinsCT
ENST00000519080.1:c.460+19_460+20delinsCT	ENSP00000428337.1:n.460+19_460+20delinsCT
ENST00000519097.5:c.589+19_589+20delinsCT	ENSP00000430686.1:n.589+19_589+20delinsCT
ENST00000615002.4:c.901+19_901+20delinsCT	ENSP00000480251.1:n.901+19_901+20delinsCT
NM_000459.4:c.901+19_901+20delinsCT	NP_000450.2:n.901+19_901+20delinsCT
NM_001290077.1:c.901+19_901+20delinsCT	NP_001277006.1:n.901+19_901+20delinsCT
NM_001290078.1:c.589+19_589+20delinsCT	NP_001277007.1:n.589+19_589+20delinsCT
XM_005251561.1:c.901+19_901+20delinsCT	XP_005251618.1:n.901+19_901+20delinsCT
XM_005251563.1:c.901+19_901+20delinsCT	XP_005251620.1:n.901+19_901+20delinsCT
XM_005251561.2:c.901+19_901+20delinsCT	XP_005251618.1:n.901+19_901+20delinsCT
XM_005251563.2:c.901+19_901+20delinsCT	XP_005251620.1:n.901+19_901+20delinsCT
NM_000459.5:c.901+19_901+20delinsCT MANE Select	NP_000450.3:n.901+19_901+20delinsCT
NM_001375475.1:c.901+19_901+20delinsCT	NP_001362404.1:n.901+19_901+20delinsCT
NM_001375476.1:c.901+19_901+20delinsCT	NP_001362405.1:n.901+19_901+20delinsCT