Canonical Allele Identifier: CA2783315750
Gene: TEK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27172932_27172933insGAG , CM000671.2:g.27172932_27172933insGAG GRCh38
NC_000009.11:g.27172930_27172931insGAG , CM000671.1:g.27172930_27172931insGAG GRCh37
NC_000009.10:g.27162930_27162931insGAG NCBI36
NG_011828.1:g.68784_68785insGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000380036.10:c.760+185_760+186insGAG MANE Select ENSP00000369375.4:n.760+185_760+186insGAG
ENST00000380036.8:c.760+185_760+186insGAG ENSP00000369375.4:n.760+185_760+186insGAG
ENST00000406359.8:c.760+185_760+186insGAG ENSP00000383977.4:n.760+185_760+186insGAG
ENST00000519080.1:c.319+185_319+186insGAG ENSP00000428337.1:n.319+185_319+186insGAG
ENST00000519097.5:c.448+185_448+186insGAG ENSP00000430686.1:n.448+185_448+186insGAG
ENST00000615002.4:c.760+185_760+186insGAG ENSP00000480251.1:n.760+185_760+186insGAG
NM_000459.4:c.760+185_760+186insGAG NP_000450.2:n.760+185_760+186insGAG
NM_001290077.1:c.760+185_760+186insGAG NP_001277006.1:n.760+185_760+186insGAG
NM_001290078.1:c.448+185_448+186insGAG NP_001277007.1:n.448+185_448+186insGAG
XM_005251561.1:c.760+185_760+186insGAG XP_005251618.1:n.760+185_760+186insGAG
XM_005251563.1:c.760+185_760+186insGAG XP_005251620.1:n.760+185_760+186insGAG
XM_005251561.2:c.760+185_760+186insGAG XP_005251618.1:n.760+185_760+186insGAG
XM_005251563.2:c.760+185_760+186insGAG XP_005251620.1:n.760+185_760+186insGAG
NM_000459.5:c.760+185_760+186insGAG MANE Select NP_000450.3:n.760+185_760+186insGAG
NM_001375475.1:c.760+185_760+186insGAG NP_001362404.1:n.760+185_760+186insGAG
NM_001375476.1:c.760+185_760+186insGAG NP_001362405.1:n.760+185_760+186insGAG