Canonical Allele Identifier: CA1842004475

Gene: TEK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27204862T= , CM000671.2:g.27204862T=	GRCh38
NC_000009.11:g.27204860T= , CM000671.1:g.27204860T=	GRCh37
NC_000009.10:g.27194860T=	NCBI36
NG_011828.1:g.100714T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.2210-49T= MANE Select	ENSP00000369375.4:n.2210-49T=
ENST00000380036.8:c.2210-49T=	ENSP00000369375.4:n.2210-49T=
ENST00000406359.8:c.2081-49T=	ENSP00000383977.4:n.2081-49T=
ENST00000519097.5:c.1769-49T=	ENSP00000430686.1:n.1769-49T=
ENST00000615002.4:c.*711-49T=	ENSP00000480251.1:n.*711-49T=
NM_000459.4:c.2210-49T=	NP_000450.2:n.2210-49T=
NM_001290077.1:c.2081-49T=	NP_001277006.1:n.2081-49T=
NM_001290078.1:c.1769-49T=	NP_001277007.1:n.1769-49T=
XM_005251561.1:c.2210-49T=	XP_005251618.1:n.2210-49T=
XM_005251563.1:c.2081-49T=	XP_005251620.1:n.2081-49T=
XM_005251561.2:c.2210-49T=	XP_005251618.1:n.2210-49T=
XM_005251563.2:c.2081-49T=	XP_005251620.1:n.2081-49T=
NM_000459.5:c.2210-49T= MANE Select	NP_000450.3:n.2210-49T=
NM_001375475.1:c.2210-49T=	NP_001362404.1:n.2210-49T=
NM_001375476.1:c.2081-49T=	NP_001362405.1:n.2081-49T=