Canonical Allele Identifier: CA1842008673

Gene: TEK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27212783G= , CM000671.2:g.27212783G=	GRCh38
NC_000009.11:g.27212781G= , CM000671.1:g.27212781G=	GRCh37
NC_000009.10:g.27202781G=	NCBI36
NG_011828.1:g.108635G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.2763G= MANE Select	ENSP00000369375.4:p.Glu921=
ENST00000380036.8:c.2763G=	ENSP00000369375.4:p.Glu921=
ENST00000406359.8:c.2634G=	ENSP00000383977.4:p.Glu878=
ENST00000519097.5:c.2319G=	ENSP00000430686.1:p.Glu773=
ENST00000615002.4:c.*1264G=	ENSP00000480251.1:n.*1264G=
NM_000459.4:c.2763G=	NP_000450.2:p.Glu921=
NM_001290077.1:c.2634G=	NP_001277006.1:p.Glu878=
NM_001290078.1:c.2319G=	NP_001277007.1:p.Glu773=
XM_005251561.1:c.2760G=	XP_005251618.1:p.Glu920=
XM_005251563.1:c.2631G=	XP_005251620.1:p.Glu877=
XM_005251561.2:c.2760G=	XP_005251618.1:p.Glu920=
XM_005251563.2:c.2631G=	XP_005251620.1:p.Glu877=
NM_000459.5:c.2763G= MANE Select	NP_000450.3:p.Glu921=
NM_001375475.1:c.2760G=	NP_001362404.1:p.Glu920=
NM_001375476.1:c.2631G=	NP_001362405.1:p.Glu877=