Canonical Allele Identifier: CA373122668

Gene: TEK

Linked Data

• MyVariant Identifiers: chr9:g.27212705G>T (hg19) ; chr9:g.27212707G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27212707G>T , CM000671.2:g.27212707G>T	GRCh38
NC_000009.11:g.27212705G>T , CM000671.1:g.27212705G>T	GRCh37
NC_000009.10:g.27202705G>T	NCBI36
NG_011828.1:g.108559G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.2687G>T MANE Select	ENSP00000369375.4:p.Gly896Val
ENST00000380036.8:c.2687G>T	ENSP00000369375.4:p.Gly896Val
ENST00000406359.8:c.2558G>T	ENSP00000383977.4:p.Gly853Val
ENST00000519097.5:c.2243G>T	ENSP00000430686.1:p.Gly748Val
ENST00000615002.4:c.*1188G>T	ENSP00000480251.1:n.*1188G>T
NM_000459.4:c.2687G>T	NP_000450.2:p.Gly896Val
NM_001290077.1:c.2558G>T	NP_001277006.1:p.Gly853Val
NM_001290078.1:c.2243G>T	NP_001277007.1:p.Gly748Val
XM_005251561.1:c.2684G>T	XP_005251618.1:p.Gly895Val
XM_005251563.1:c.2555G>T	XP_005251620.1:p.Gly852Val
XM_005251561.2:c.2684G>T	XP_005251618.1:p.Gly895Val
XM_005251563.2:c.2555G>T	XP_005251620.1:p.Gly852Val
NM_000459.5:c.2687G>T MANE Select	NP_000450.3:p.Gly896Val
NM_001375475.1:c.2684G>T	NP_001362404.1:p.Gly895Val
NM_001375476.1:c.2555G>T	NP_001362405.1:p.Gly852Val