Canonical Allele Identifier: CA1842021647

Gene: TEK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27173262G= , CM000671.2:g.27173262G=	GRCh38
NC_000009.11:g.27173260G= , CM000671.1:g.27173260G=	GRCh37
NC_000009.10:g.27163260G=	NCBI36
NG_011828.1:g.69114G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.801G= MANE Select	ENSP00000369375.4:p.Arg267=
ENST00000380036.8:c.801G=	ENSP00000369375.4:p.Arg267=
ENST00000406359.8:c.801G=	ENSP00000383977.4:p.Arg267=
ENST00000519080.1:c.360G=	ENSP00000428337.1:p.Arg120=
ENST00000519097.5:c.489G=	ENSP00000430686.1:p.Arg163=
ENST00000615002.4:c.801G=	ENSP00000480251.1:p.Arg267=
NM_000459.4:c.801G=	NP_000450.2:p.Arg267=
NM_001290077.1:c.801G=	NP_001277006.1:p.Arg267=
NM_001290078.1:c.489G=	NP_001277007.1:p.Arg163=
XM_005251561.1:c.801G=	XP_005251618.1:p.Arg267=
XM_005251563.1:c.801G=	XP_005251620.1:p.Arg267=
XM_005251561.2:c.801G=	XP_005251618.1:p.Arg267=
XM_005251563.2:c.801G=	XP_005251620.1:p.Arg267=
NM_000459.5:c.801G= MANE Select	NP_000450.3:p.Arg267=
NM_001375475.1:c.801G=	NP_001362404.1:p.Arg267=
NM_001375476.1:c.801G=	NP_001362405.1:p.Arg267=