Canonical Allele Identifier: CA464169944

Gene: TEK

Linked Data

• MyVariant Identifiers: chr9:g.27212754C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27212756C>T , CM000671.2:g.27212756C>T	GRCh38
NC_000009.11:g.27212754C>T , CM000671.1:g.27212754C>T	GRCh37
NC_000009.10:g.27202754C>T	NCBI36
NG_011828.1:g.108608C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.2736C>T MANE Select	ENSP00000369375.4:p.Asp912=
ENST00000380036.8:c.2736C>T	ENSP00000369375.4:p.Asp912=
ENST00000406359.8:c.2607C>T	ENSP00000383977.4:p.Asp869=
ENST00000519097.5:c.2292C>T	ENSP00000430686.1:p.Asp764=
ENST00000615002.4:c.*1237C>T	ENSP00000480251.1:n.*1237C>T
NM_000459.4:c.2736C>T	NP_000450.2:p.Asp912=
NM_001290077.1:c.2607C>T	NP_001277006.1:p.Asp869=
NM_001290078.1:c.2292C>T	NP_001277007.1:p.Asp764=
XM_005251561.1:c.2733C>T	XP_005251618.1:p.Asp911=
XM_005251563.1:c.2604C>T	XP_005251620.1:p.Asp868=
XM_005251561.2:c.2733C>T	XP_005251618.1:p.Asp911=
XM_005251563.2:c.2604C>T	XP_005251620.1:p.Asp868=
NM_000459.5:c.2736C>T MANE Select	NP_000450.3:p.Asp912=
NM_001375475.1:c.2733C>T	NP_001362404.1:p.Asp911=
NM_001375476.1:c.2604C>T	NP_001362405.1:p.Asp868=