Canonical Allele Identifier: CA1842005384

Gene: TEK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27206762C= , CM000671.2:g.27206762C=	GRCh38
NC_000009.11:g.27206760C= , CM000671.1:g.27206760C=	GRCh37
NC_000009.10:g.27196760C=	NCBI36
NG_011828.1:g.102614C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000459.5:c.2545C= MANE Select	NP_000450.3:p.Arg849=
ENST00000380036.10:c.2545C= MANE Select	ENSP00000369375.4:p.Arg849=
NM_000459.4:c.2545C=	NP_000450.2:p.Arg849=
NM_001290077.1:c.2416C=	NP_001277006.1:p.Arg806=
NM_001290078.1:c.2101C=	NP_001277007.1:p.Arg701=
NM_001375475.1:c.2542C=	NP_001362404.1:p.Arg848=
NM_001375476.1:c.2413C=	NP_001362405.1:p.Arg805=
ENST00000380036.8:c.2545C=	ENSP00000369375.4:p.Arg849=
ENST00000406359.8:c.2416C=	ENSP00000383977.4:p.Arg806=
ENST00000519097.5:c.2101C=	ENSP00000430686.1:p.Arg701=
ENST00000615002.4:c.*1046C=	ENSP00000480251.1:n.*1046C=
XM_005251561.1:c.2542C=	XP_005251618.1:p.Arg848=
XM_005251561.2:c.2542C=	XP_005251618.1:p.Arg848=
XM_005251563.1:c.2413C=	XP_005251620.1:p.Arg805=
XM_005251563.2:c.2413C=	XP_005251620.1:p.Arg805=