Canonical Allele Identifier: CA5016009

Gene: TEK

Linked Data

• dbSNP Id: rs757069148
• ExAC: 9:27173179 G / A
• gnomAD v2: 9-27173179-G-A
• gnomAD v3: 9-27173181-G-A
• gnomAD v4: 9-27173181-G-A
• MyVariant Identifiers: chr9:g.27173179G>A (hg19) ; chr9:g.27173181G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27173181G>A , CM000671.2:g.27173181G>A	GRCh38
NC_000009.11:g.27173179G>A , CM000671.1:g.27173179G>A	GRCh37
NC_000009.10:g.27163179G>A	NCBI36
NG_011828.1:g.69033G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000380036.10:c.761-41G>A MANE Select	ENSP00000369375.4:n.761-41G>A
ENST00000380036.8:c.761-41G>A	ENSP00000369375.4:n.761-41G>A
ENST00000406359.8:c.761-41G>A	ENSP00000383977.4:n.761-41G>A
ENST00000519080.1:c.320-41G>A	ENSP00000428337.1:n.320-41G>A
ENST00000519097.5:c.449-41G>A	ENSP00000430686.1:n.449-41G>A
ENST00000615002.4:c.761-41G>A	ENSP00000480251.1:n.761-41G>A
NM_000459.4:c.761-41G>A	NP_000450.2:n.761-41G>A
NM_001290077.1:c.761-41G>A	NP_001277006.1:n.761-41G>A
NM_001290078.1:c.449-41G>A	NP_001277007.1:n.449-41G>A
XM_005251561.1:c.761-41G>A	XP_005251618.1:n.761-41G>A
XM_005251563.1:c.761-41G>A	XP_005251620.1:n.761-41G>A
XM_005251561.2:c.761-41G>A	XP_005251618.1:n.761-41G>A
XM_005251563.2:c.761-41G>A	XP_005251620.1:n.761-41G>A
NM_000459.5:c.761-41G>A MANE Select	NP_000450.3:n.761-41G>A
NM_001375475.1:c.761-41G>A	NP_001362404.1:n.761-41G>A
NM_001375476.1:c.761-41G>A	NP_001362405.1:n.761-41G>A