Canonical Allele Identifier: CA1842008665

Gene: TEK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27212758T= , CM000671.2:g.27212758T=	GRCh38
NC_000009.11:g.27212756T= , CM000671.1:g.27212756T=	GRCh37
NC_000009.10:g.27202756T=	NCBI36
NG_011828.1:g.108610T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.2738T= MANE Select	ENSP00000369375.4:p.Phe913=
ENST00000380036.8:c.2738T=	ENSP00000369375.4:p.Phe913=
ENST00000406359.8:c.2609T=	ENSP00000383977.4:p.Phe870=
ENST00000519097.5:c.2294T=	ENSP00000430686.1:p.Phe765=
ENST00000615002.4:c.*1239T=	ENSP00000480251.1:n.*1239T=
NM_000459.4:c.2738T=	NP_000450.2:p.Phe913=
NM_001290077.1:c.2609T=	NP_001277006.1:p.Phe870=
NM_001290078.1:c.2294T=	NP_001277007.1:p.Phe765=
XM_005251561.1:c.2735T=	XP_005251618.1:p.Phe912=
XM_005251563.1:c.2606T=	XP_005251620.1:p.Phe869=
XM_005251561.2:c.2735T=	XP_005251618.1:p.Phe912=
XM_005251563.2:c.2606T=	XP_005251620.1:p.Phe869=
NM_000459.5:c.2738T= MANE Select	NP_000450.3:p.Phe913=
NM_001375475.1:c.2735T=	NP_001362404.1:p.Phe912=
NM_001375476.1:c.2606T=	NP_001362405.1:p.Phe869=