Canonical Allele Identifier: CA373122832

Gene: TEK

Linked Data

• MyVariant Identifiers: chr9:g.27212740G>T (hg19) ; chr9:g.27212742G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27212742G>T , CM000671.2:g.27212742G>T	GRCh38
NC_000009.11:g.27212740G>T , CM000671.1:g.27212740G>T	GRCh37
NC_000009.10:g.27202740G>T	NCBI36
NG_011828.1:g.108594G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.2722G>T MANE Select	ENSP00000369375.4:p.Gly908Ter
ENST00000380036.8:c.2722G>T	ENSP00000369375.4:p.Gly908Ter
ENST00000406359.8:c.2593G>T	ENSP00000383977.4:p.Gly865Ter
ENST00000519097.5:c.2278G>T	ENSP00000430686.1:p.Gly760Ter
ENST00000615002.4:c.*1223G>T	ENSP00000480251.1:n.*1223G>T
NM_000459.4:c.2722G>T	NP_000450.2:p.Gly908Ter
NM_001290077.1:c.2593G>T	NP_001277006.1:p.Gly865Ter
NM_001290078.1:c.2278G>T	NP_001277007.1:p.Gly760Ter
XM_005251561.1:c.2719G>T	XP_005251618.1:p.Gly907Ter
XM_005251563.1:c.2590G>T	XP_005251620.1:p.Gly864Ter
XM_005251561.2:c.2719G>T	XP_005251618.1:p.Gly907Ter
XM_005251563.2:c.2590G>T	XP_005251620.1:p.Gly864Ter
NM_000459.5:c.2722G>T MANE Select	NP_000450.3:p.Gly908Ter
NM_001375475.1:c.2719G>T	NP_001362404.1:p.Gly907Ter
NM_001375476.1:c.2590G>T	NP_001362405.1:p.Gly864Ter