Canonical Allele Identifier: CA464170043

Gene: TEK

Linked Data

• MyVariant Identifiers: chr9:g.27183482A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27183484A>T , CM000671.2:g.27183484A>T	GRCh38
NC_000009.11:g.27183482A>T , CM000671.1:g.27183482A>T	GRCh37
NC_000009.10:g.27173482A>T	NCBI36
NG_011828.1:g.79336A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.1056A>T MANE Select	ENSP00000369375.4:p.Ile352=
ENST00000380036.8:c.1056A>T	ENSP00000369375.4:p.Ile352=
ENST00000406359.8:c.927A>T	ENSP00000383977.4:p.Ile309=
ENST00000519080.1:c.486A>T	ENSP00000428337.1:p.Ile162=
ENST00000519097.5:c.615A>T	ENSP00000430686.1:p.Ile205=
ENST00000615002.4:c.927A>T	ENSP00000480251.1:p.Ile309=
NM_000459.4:c.1056A>T	NP_000450.2:p.Ile352=
NM_001290077.1:c.927A>T	NP_001277006.1:p.Ile309=
NM_001290078.1:c.615A>T	NP_001277007.1:p.Ile205=
XM_005251561.1:c.1056A>T	XP_005251618.1:p.Ile352=
XM_005251563.1:c.927A>T	XP_005251620.1:p.Ile309=
XM_005251561.2:c.1056A>T	XP_005251618.1:p.Ile352=
XM_005251563.2:c.927A>T	XP_005251620.1:p.Ile309=
NM_000459.5:c.1056A>T MANE Select	NP_000450.3:p.Ile352=
NM_001375475.1:c.1056A>T	NP_001362404.1:p.Ile352=
NM_001375476.1:c.927A>T	NP_001362405.1:p.Ile309=