Canonical Allele Identifier: CA464168713

Gene: TEK

Linked Data

• MyVariant Identifiers: chr9:g.27173323C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27173325C>G , CM000671.2:g.27173325C>G	GRCh38
NC_000009.11:g.27173323C>G , CM000671.1:g.27173323C>G	GRCh37
NC_000009.10:g.27163323C>G	NCBI36
NG_011828.1:g.69177C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.864C>G MANE Select	ENSP00000369375.4:p.Ser288=
ENST00000380036.8:c.864C>G	ENSP00000369375.4:p.Ser288=
ENST00000406359.8:c.864C>G	ENSP00000383977.4:p.Ser288=
ENST00000519080.1:c.423C>G	ENSP00000428337.1:p.Ser141=
ENST00000519097.5:c.552C>G	ENSP00000430686.1:p.Ser184=
ENST00000615002.4:c.864C>G	ENSP00000480251.1:p.Ser288=
NM_000459.4:c.864C>G	NP_000450.2:p.Ser288=
NM_001290077.1:c.864C>G	NP_001277006.1:p.Ser288=
NM_001290078.1:c.552C>G	NP_001277007.1:p.Ser184=
XM_005251561.1:c.864C>G	XP_005251618.1:p.Ser288=
XM_005251563.1:c.864C>G	XP_005251620.1:p.Ser288=
XM_005251561.2:c.864C>G	XP_005251618.1:p.Ser288=
XM_005251563.2:c.864C>G	XP_005251620.1:p.Ser288=
NM_000459.5:c.864C>G MANE Select	NP_000450.3:p.Ser288=
NM_001375475.1:c.864C>G	NP_001362404.1:p.Ser288=
NM_001375476.1:c.864C>G	NP_001362405.1:p.Ser288=