Canonical Allele Identifier: CA1842021669

Gene: TEK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27173275G= , CM000671.2:g.27173275G=	GRCh38
NC_000009.11:g.27173273G= , CM000671.1:g.27173273G=	GRCh37
NC_000009.10:g.27163273G=	NCBI36
NG_011828.1:g.69127G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.814G= MANE Select	ENSP00000369375.4:p.Glu272=
ENST00000380036.8:c.814G=	ENSP00000369375.4:p.Glu272=
ENST00000406359.8:c.814G=	ENSP00000383977.4:p.Glu272=
ENST00000519080.1:c.373G=	ENSP00000428337.1:p.Glu125=
ENST00000519097.5:c.502G=	ENSP00000430686.1:p.Glu168=
ENST00000615002.4:c.814G=	ENSP00000480251.1:p.Glu272=
NM_000459.4:c.814G=	NP_000450.2:p.Glu272=
NM_001290077.1:c.814G=	NP_001277006.1:p.Glu272=
NM_001290078.1:c.502G=	NP_001277007.1:p.Glu168=
XM_005251561.1:c.814G=	XP_005251618.1:p.Glu272=
XM_005251563.1:c.814G=	XP_005251620.1:p.Glu272=
XM_005251561.2:c.814G=	XP_005251618.1:p.Glu272=
XM_005251563.2:c.814G=	XP_005251620.1:p.Glu272=
NM_000459.5:c.814G= MANE Select	NP_000450.3:p.Glu272=
NM_001375475.1:c.814G=	NP_001362404.1:p.Glu272=
NM_001375476.1:c.814G=	NP_001362405.1:p.Glu272=