Canonical Allele Identifier: CA1842021081

Gene: TEK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27172897_27172898delinsCT , CM000671.2:g.27172897_27172898delinsCT	GRCh38
NC_000009.11:g.27172895_27172896delinsCT , CM000671.1:g.27172895_27172896delinsCT	GRCh37
NC_000009.10:g.27162895_27162896delinsCT	NCBI36
NG_011828.1:g.68749_68750delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.760+150_760+151delinsCT MANE Select	ENSP00000369375.4:n.760+150_760+151delinsCT
ENST00000380036.8:c.760+150_760+151delinsCT	ENSP00000369375.4:n.760+150_760+151delinsCT
ENST00000406359.8:c.760+150_760+151delinsCT	ENSP00000383977.4:n.760+150_760+151delinsCT
ENST00000519080.1:c.319+150_319+151delinsCT	ENSP00000428337.1:n.319+150_319+151delinsCT
ENST00000519097.5:c.448+150_448+151delinsCT	ENSP00000430686.1:n.448+150_448+151delinsCT
ENST00000615002.4:c.760+150_760+151delinsCT	ENSP00000480251.1:n.760+150_760+151delinsCT
NM_000459.4:c.760+150_760+151delinsCT	NP_000450.2:n.760+150_760+151delinsCT
NM_001290077.1:c.760+150_760+151delinsCT	NP_001277006.1:n.760+150_760+151delinsCT
NM_001290078.1:c.448+150_448+151delinsCT	NP_001277007.1:n.448+150_448+151delinsCT
XM_005251561.1:c.760+150_760+151delinsCT	XP_005251618.1:n.760+150_760+151delinsCT
XM_005251563.1:c.760+150_760+151delinsCT	XP_005251620.1:n.760+150_760+151delinsCT
XM_005251561.2:c.760+150_760+151delinsCT	XP_005251618.1:n.760+150_760+151delinsCT
XM_005251563.2:c.760+150_760+151delinsCT	XP_005251620.1:n.760+150_760+151delinsCT
NM_000459.5:c.760+150_760+151delinsCT MANE Select	NP_000450.3:n.760+150_760+151delinsCT
NM_001375475.1:c.760+150_760+151delinsCT	NP_001362404.1:n.760+150_760+151delinsCT
NM_001375476.1:c.760+150_760+151delinsCT	NP_001362405.1:n.760+150_760+151delinsCT