Canonical Allele Identifier: CA464170007

Gene: TEK

Linked Data

• MyVariant Identifiers: chr9:g.27183461A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27183463A>T , CM000671.2:g.27183463A>T	GRCh38
NC_000009.11:g.27183461A>T , CM000671.1:g.27183461A>T	GRCh37
NC_000009.10:g.27173461A>T	NCBI36
NG_011828.1:g.79315A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.1035A>T MANE Select	ENSP00000369375.4:p.Ile345=
ENST00000380036.8:c.1035A>T	ENSP00000369375.4:p.Ile345=
ENST00000406359.8:c.906A>T	ENSP00000383977.4:p.Ile302=
ENST00000519080.1:c.465A>T	ENSP00000428337.1:p.Ile155=
ENST00000519097.5:c.594A>T	ENSP00000430686.1:p.Ile198=
ENST00000615002.4:c.906A>T	ENSP00000480251.1:p.Ile302=
NM_000459.4:c.1035A>T	NP_000450.2:p.Ile345=
NM_001290077.1:c.906A>T	NP_001277006.1:p.Ile302=
NM_001290078.1:c.594A>T	NP_001277007.1:p.Ile198=
XM_005251561.1:c.1035A>T	XP_005251618.1:p.Ile345=
XM_005251563.1:c.906A>T	XP_005251620.1:p.Ile302=
XM_005251561.2:c.1035A>T	XP_005251618.1:p.Ile345=
XM_005251563.2:c.906A>T	XP_005251620.1:p.Ile302=
NM_000459.5:c.1035A>T MANE Select	NP_000450.3:p.Ile345=
NM_001375475.1:c.1035A>T	NP_001362404.1:p.Ile345=
NM_001375476.1:c.906A>T	NP_001362405.1:p.Ile302=