Canonical Allele Identifier: CA1842021859

Gene: TEK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27173391_27173394delinsGGAT , CM000671.2:g.27173391_27173394delinsGGAT	GRCh38
NC_000009.11:g.27173389_27173392delinsGGAT , CM000671.1:g.27173389_27173392delinsGGAT	GRCh37
NC_000009.10:g.27163389_27163392delinsGGAT	NCBI36
NG_011828.1:g.69243_69246delinsGGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.901+29_901+32delinsGGAT MANE Select	ENSP00000369375.4:n.901+29_901+32delinsGGAT
ENST00000380036.8:c.901+29_901+32delinsGGAT	ENSP00000369375.4:n.901+29_901+32delinsGGAT
ENST00000406359.8:c.901+29_901+32delinsGGAT	ENSP00000383977.4:n.901+29_901+32delinsGGAT
ENST00000519080.1:c.460+29_460+32delinsGGAT	ENSP00000428337.1:n.460+29_460+32delinsGGAT
ENST00000519097.5:c.589+29_589+32delinsGGAT	ENSP00000430686.1:n.589+29_589+32delinsGGAT
ENST00000615002.4:c.901+29_901+32delinsGGAT	ENSP00000480251.1:n.901+29_901+32delinsGGAT
NM_000459.4:c.901+29_901+32delinsGGAT	NP_000450.2:n.901+29_901+32delinsGGAT
NM_001290077.1:c.901+29_901+32delinsGGAT	NP_001277006.1:n.901+29_901+32delinsGGAT
NM_001290078.1:c.589+29_589+32delinsGGAT	NP_001277007.1:n.589+29_589+32delinsGGAT
XM_005251561.1:c.901+29_901+32delinsGGAT	XP_005251618.1:n.901+29_901+32delinsGGAT
XM_005251563.1:c.901+29_901+32delinsGGAT	XP_005251620.1:n.901+29_901+32delinsGGAT
XM_005251561.2:c.901+29_901+32delinsGGAT	XP_005251618.1:n.901+29_901+32delinsGGAT
XM_005251563.2:c.901+29_901+32delinsGGAT	XP_005251620.1:n.901+29_901+32delinsGGAT
NM_000459.5:c.901+29_901+32delinsGGAT MANE Select	NP_000450.3:n.901+29_901+32delinsGGAT
NM_001375475.1:c.901+29_901+32delinsGGAT	NP_001362404.1:n.901+29_901+32delinsGGAT
NM_001375476.1:c.901+29_901+32delinsGGAT	NP_001362405.1:n.901+29_901+32delinsGGAT