Canonical Allele Identifier: CA373122780

Gene: TEK

Linked Data

• MyVariant Identifiers: chr9:g.27212732C>A (hg19) ; chr9:g.27212734C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27212734C>A , CM000671.2:g.27212734C>A	GRCh38
NC_000009.11:g.27212732C>A , CM000671.1:g.27212732C>A	GRCh37
NC_000009.10:g.27202732C>A	NCBI36
NG_011828.1:g.108586C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.2714C>A MANE Select	ENSP00000369375.4:p.Ala905Glu
ENST00000380036.8:c.2714C>A	ENSP00000369375.4:p.Ala905Glu
ENST00000406359.8:c.2585C>A	ENSP00000383977.4:p.Ala862Glu
ENST00000519097.5:c.2270C>A	ENSP00000430686.1:p.Ala757Glu
ENST00000615002.4:c.*1215C>A	ENSP00000480251.1:n.*1215C>A
NM_000459.4:c.2714C>A	NP_000450.2:p.Ala905Glu
NM_001290077.1:c.2585C>A	NP_001277006.1:p.Ala862Glu
NM_001290078.1:c.2270C>A	NP_001277007.1:p.Ala757Glu
XM_005251561.1:c.2711C>A	XP_005251618.1:p.Ala904Glu
XM_005251563.1:c.2582C>A	XP_005251620.1:p.Ala861Glu
XM_005251561.2:c.2711C>A	XP_005251618.1:p.Ala904Glu
XM_005251563.2:c.2582C>A	XP_005251620.1:p.Ala861Glu
NM_000459.5:c.2714C>A MANE Select	NP_000450.3:p.Ala905Glu
NM_001375475.1:c.2711C>A	NP_001362404.1:p.Ala904Glu
NM_001375476.1:c.2582C>A	NP_001362405.1:p.Ala861Glu