Canonical Allele Identifier: CA2783322708

Gene: TEK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27173502_27173503insC , CM000671.2:g.27173502_27173503insC	GRCh38
NC_000009.11:g.27173500_27173501insC , CM000671.1:g.27173500_27173501insC	GRCh37
NC_000009.10:g.27163500_27163501insC	NCBI36
NG_011828.1:g.69354_69355insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.901+140_901+141insC MANE Select	ENSP00000369375.4:n.901+140_901+141insC
ENST00000380036.8:c.901+140_901+141insC	ENSP00000369375.4:n.901+140_901+141insC
ENST00000406359.8:c.901+140_901+141insC	ENSP00000383977.4:n.901+140_901+141insC
ENST00000519080.1:c.460+140_460+141insC	ENSP00000428337.1:n.460+140_460+141insC
ENST00000519097.5:c.589+140_589+141insC	ENSP00000430686.1:n.589+140_589+141insC
ENST00000615002.4:c.901+140_901+141insC	ENSP00000480251.1:n.901+140_901+141insC
NM_000459.4:c.901+140_901+141insC	NP_000450.2:n.901+140_901+141insC
NM_001290077.1:c.901+140_901+141insC	NP_001277006.1:n.901+140_901+141insC
NM_001290078.1:c.589+140_589+141insC	NP_001277007.1:n.589+140_589+141insC
XM_005251561.1:c.901+140_901+141insC	XP_005251618.1:n.901+140_901+141insC
XM_005251563.1:c.901+140_901+141insC	XP_005251620.1:n.901+140_901+141insC
XM_005251561.2:c.901+140_901+141insC	XP_005251618.1:n.901+140_901+141insC
XM_005251563.2:c.901+140_901+141insC	XP_005251620.1:n.901+140_901+141insC
NM_000459.5:c.901+140_901+141insC MANE Select	NP_000450.3:n.901+140_901+141insC
NM_001375475.1:c.901+140_901+141insC	NP_001362404.1:n.901+140_901+141insC
NM_001375476.1:c.901+140_901+141insC	NP_001362405.1:n.901+140_901+141insC