Canonical Allele Identifier: CA464170068

Gene: TEK

Linked Data

• MyVariant Identifiers: chr9:g.27183497T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27183499T>C , CM000671.2:g.27183499T>C	GRCh38
NC_000009.11:g.27183497T>C , CM000671.1:g.27183497T>C	GRCh37
NC_000009.10:g.27173497T>C	NCBI36
NG_011828.1:g.79351T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.1071T>C MANE Select	ENSP00000369375.4:p.Asp357=
ENST00000380036.8:c.1071T>C	ENSP00000369375.4:p.Asp357=
ENST00000406359.8:c.942T>C	ENSP00000383977.4:p.Asp314=
ENST00000519080.1:c.501T>C	ENSP00000428337.1:p.Asp167=
ENST00000519097.5:c.630T>C	ENSP00000430686.1:p.Asp210=
ENST00000615002.4:c.942T>C	ENSP00000480251.1:p.Asp314=
NM_000459.4:c.1071T>C	NP_000450.2:p.Asp357=
NM_001290077.1:c.942T>C	NP_001277006.1:p.Asp314=
NM_001290078.1:c.630T>C	NP_001277007.1:p.Asp210=
XM_005251561.1:c.1071T>C	XP_005251618.1:p.Asp357=
XM_005251563.1:c.942T>C	XP_005251620.1:p.Asp314=
XM_005251561.2:c.1071T>C	XP_005251618.1:p.Asp357=
XM_005251563.2:c.942T>C	XP_005251620.1:p.Asp314=
NM_000459.5:c.1071T>C MANE Select	NP_000450.3:p.Asp357=
NM_001375475.1:c.1071T>C	NP_001362404.1:p.Asp357=
NM_001375476.1:c.942T>C	NP_001362405.1:p.Asp314=