Canonical Allele Identifier: CA1842030965

Gene: TEK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27183173C= , CM000671.2:g.27183173C=	GRCh38
NC_000009.11:g.27183171C= , CM000671.1:g.27183171C=	GRCh37
NC_000009.10:g.27173171C=	NCBI36
NG_011828.1:g.79025C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.1031-286C= MANE Select	ENSP00000369375.4:n.1031-286C=
ENST00000380036.8:c.1031-286C=	ENSP00000369375.4:n.1031-286C=
ENST00000406359.8:c.902-286C=	ENSP00000383977.4:n.902-286C=
ENST00000519080.1:c.461-286C=	ENSP00000428337.1:n.461-286C=
ENST00000519097.5:c.590-286C=	ENSP00000430686.1:n.590-286C=
ENST00000615002.4:c.902-286C=	ENSP00000480251.1:n.902-286C=
NM_000459.4:c.1031-286C=	NP_000450.2:n.1031-286C=
NM_001290077.1:c.902-286C=	NP_001277006.1:n.902-286C=
NM_001290078.1:c.590-286C=	NP_001277007.1:n.590-286C=
XM_005251561.1:c.1031-286C=	XP_005251618.1:n.1031-286C=
XM_005251563.1:c.902-286C=	XP_005251620.1:n.902-286C=
XM_005251561.2:c.1031-286C=	XP_005251618.1:n.1031-286C=
XM_005251563.2:c.902-286C=	XP_005251620.1:n.902-286C=
NM_000459.5:c.1031-286C= MANE Select	NP_000450.3:n.1031-286C=
NM_001375475.1:c.1031-286C=	NP_001362404.1:n.1031-286C=
NM_001375476.1:c.902-286C=	NP_001362405.1:n.902-286C=