Canonical Allele Identifier: CA373122947

Gene: TEK

Linked Data

• MyVariant Identifiers: chr9:g.27212758C>A (hg19) ; chr9:g.27212760C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27212760C>A , CM000671.2:g.27212760C>A	GRCh38
NC_000009.11:g.27212758C>A , CM000671.1:g.27212758C>A	GRCh37
NC_000009.10:g.27202758C>A	NCBI36
NG_011828.1:g.108612C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.2740C>A MANE Select	ENSP00000369375.4:p.Leu914Ile
ENST00000380036.8:c.2740C>A	ENSP00000369375.4:p.Leu914Ile
ENST00000406359.8:c.2611C>A	ENSP00000383977.4:p.Leu871Ile
ENST00000519097.5:c.2296C>A	ENSP00000430686.1:p.Leu766Ile
ENST00000615002.4:c.*1241C>A	ENSP00000480251.1:n.*1241C>A
NM_000459.4:c.2740C>A	NP_000450.2:p.Leu914Ile
NM_001290077.1:c.2611C>A	NP_001277006.1:p.Leu871Ile
NM_001290078.1:c.2296C>A	NP_001277007.1:p.Leu766Ile
XM_005251561.1:c.2737C>A	XP_005251618.1:p.Leu913Ile
XM_005251563.1:c.2608C>A	XP_005251620.1:p.Leu870Ile
XM_005251561.2:c.2737C>A	XP_005251618.1:p.Leu913Ile
XM_005251563.2:c.2608C>A	XP_005251620.1:p.Leu870Ile
NM_000459.5:c.2740C>A MANE Select	NP_000450.3:p.Leu914Ile
NM_001375475.1:c.2737C>A	NP_001362404.1:p.Leu913Ile
NM_001375476.1:c.2608C>A	NP_001362405.1:p.Leu870Ile