Canonical Allele Identifier: CA464170002

Gene: TEK

Linked Data

• MyVariant Identifiers: chr9:g.27183458C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27183460C>G , CM000671.2:g.27183460C>G	GRCh38
NC_000009.11:g.27183458C>G , CM000671.1:g.27183458C>G	GRCh37
NC_000009.10:g.27173458C>G	NCBI36
NG_011828.1:g.79312C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.1032C>G MANE Select	ENSP00000369375.4:p.Gly344=
ENST00000380036.8:c.1032C>G	ENSP00000369375.4:p.Gly344=
ENST00000406359.8:c.903C>G	ENSP00000383977.4:p.Gly301=
ENST00000519080.1:c.462C>G	ENSP00000428337.1:p.Gly154=
ENST00000519097.5:c.591C>G	ENSP00000430686.1:p.Gly197=
ENST00000615002.4:c.903C>G	ENSP00000480251.1:p.Gly301=
NM_000459.4:c.1032C>G	NP_000450.2:p.Gly344=
NM_001290077.1:c.903C>G	NP_001277006.1:p.Gly301=
NM_001290078.1:c.591C>G	NP_001277007.1:p.Gly197=
XM_005251561.1:c.1032C>G	XP_005251618.1:p.Gly344=
XM_005251563.1:c.903C>G	XP_005251620.1:p.Gly301=
XM_005251561.2:c.1032C>G	XP_005251618.1:p.Gly344=
XM_005251563.2:c.903C>G	XP_005251620.1:p.Gly301=
NM_000459.5:c.1032C>G MANE Select	NP_000450.3:p.Gly344=
NM_001375475.1:c.1032C>G	NP_001362404.1:p.Gly344=
NM_001375476.1:c.903C>G	NP_001362405.1:p.Gly301=