Canonical Allele Identifier: CA373125165

Gene: TEK

Linked Data

• MyVariant Identifiers: chr9:g.27173244G>A (hg19) ; chr9:g.27173246G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27173246G>A , CM000671.2:g.27173246G>A	GRCh38
NC_000009.11:g.27173244G>A , CM000671.1:g.27173244G>A	GRCh37
NC_000009.10:g.27163244G>A	NCBI36
NG_011828.1:g.69098G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000380036.10:c.785G>A MANE Select	ENSP00000369375.4:p.Arg262Lys
ENST00000380036.8:c.785G>A	ENSP00000369375.4:p.Arg262Lys
ENST00000406359.8:c.785G>A	ENSP00000383977.4:p.Arg262Lys
ENST00000519080.1:c.344G>A	ENSP00000428337.1:p.Arg115Lys
ENST00000519097.5:c.473G>A	ENSP00000430686.1:p.Arg158Lys
ENST00000615002.4:c.785G>A	ENSP00000480251.1:p.Arg262Lys
NM_000459.4:c.785G>A	NP_000450.2:p.Arg262Lys
NM_001290077.1:c.785G>A	NP_001277006.1:p.Arg262Lys
NM_001290078.1:c.473G>A	NP_001277007.1:p.Arg158Lys
XM_005251561.1:c.785G>A	XP_005251618.1:p.Arg262Lys
XM_005251563.1:c.785G>A	XP_005251620.1:p.Arg262Lys
XM_005251561.2:c.785G>A	XP_005251618.1:p.Arg262Lys
XM_005251563.2:c.785G>A	XP_005251620.1:p.Arg262Lys
NM_000459.5:c.785G>A MANE Select	NP_000450.3:p.Arg262Lys
NM_001375475.1:c.785G>A	NP_001362404.1:p.Arg262Lys
NM_001375476.1:c.785G>A	NP_001362405.1:p.Arg262Lys