Canonical Allele Identifier: CA2783315613
Gene: TEK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27172836_27172837insACA , CM000671.2:g.27172836_27172837insACA GRCh38
NC_000009.11:g.27172834_27172835insACA , CM000671.1:g.27172834_27172835insACA GRCh37
NC_000009.10:g.27162834_27162835insACA NCBI36
NG_011828.1:g.68688_68689insACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000380036.10:c.760+89_760+90insACA MANE Select ENSP00000369375.4:n.760+89_760+90insACA
ENST00000380036.8:c.760+89_760+90insACA ENSP00000369375.4:n.760+89_760+90insACA
ENST00000406359.8:c.760+89_760+90insACA ENSP00000383977.4:n.760+89_760+90insACA
ENST00000519080.1:c.319+89_319+90insACA ENSP00000428337.1:n.319+89_319+90insACA
ENST00000519097.5:c.448+89_448+90insACA ENSP00000430686.1:n.448+89_448+90insACA
ENST00000615002.4:c.760+89_760+90insACA ENSP00000480251.1:n.760+89_760+90insACA
NM_000459.4:c.760+89_760+90insACA NP_000450.2:n.760+89_760+90insACA
NM_001290077.1:c.760+89_760+90insACA NP_001277006.1:n.760+89_760+90insACA
NM_001290078.1:c.448+89_448+90insACA NP_001277007.1:n.448+89_448+90insACA
XM_005251561.1:c.760+89_760+90insACA XP_005251618.1:n.760+89_760+90insACA
XM_005251563.1:c.760+89_760+90insACA XP_005251620.1:n.760+89_760+90insACA
XM_005251561.2:c.760+89_760+90insACA XP_005251618.1:n.760+89_760+90insACA
XM_005251563.2:c.760+89_760+90insACA XP_005251620.1:n.760+89_760+90insACA
NM_000459.5:c.760+89_760+90insACA MANE Select NP_000450.3:n.760+89_760+90insACA
NM_001375475.1:c.760+89_760+90insACA NP_001362404.1:n.760+89_760+90insACA
NM_001375476.1:c.760+89_760+90insACA NP_001362405.1:n.760+89_760+90insACA