Canonical Allele Identifier: CA1842021698

Gene: TEK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27173298C= , CM000671.2:g.27173298C=	GRCh38
NC_000009.11:g.27173296C= , CM000671.1:g.27173296C=	GRCh37
NC_000009.10:g.27163296C=	NCBI36
NG_011828.1:g.69150C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.837C= MANE Select	ENSP00000369375.4:p.Phe279=
ENST00000380036.8:c.837C=	ENSP00000369375.4:p.Phe279=
ENST00000406359.8:c.837C=	ENSP00000383977.4:p.Phe279=
ENST00000519080.1:c.396C=	ENSP00000428337.1:p.Phe132=
ENST00000519097.5:c.525C=	ENSP00000430686.1:p.Phe175=
ENST00000615002.4:c.837C=	ENSP00000480251.1:p.Phe279=
NM_000459.4:c.837C=	NP_000450.2:p.Phe279=
NM_001290077.1:c.837C=	NP_001277006.1:p.Phe279=
NM_001290078.1:c.525C=	NP_001277007.1:p.Phe175=
XM_005251561.1:c.837C=	XP_005251618.1:p.Phe279=
XM_005251563.1:c.837C=	XP_005251620.1:p.Phe279=
XM_005251561.2:c.837C=	XP_005251618.1:p.Phe279=
XM_005251563.2:c.837C=	XP_005251620.1:p.Phe279=
NM_000459.5:c.837C= MANE Select	NP_000450.3:p.Phe279=
NM_001375475.1:c.837C=	NP_001362404.1:p.Phe279=
NM_001375476.1:c.837C=	NP_001362405.1:p.Phe279=