Canonical Allele Identifier: CA2645441113
Gene: POMGNT1 HGNC NCBI
TSPAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46192170_46192171insGTA , CM000663.2:g.46192170_46192171insGTA GRCh38
NC_000001.10:g.46657842_46657843insGTA , CM000663.1:g.46657842_46657843insGTA GRCh37
NC_000001.9:g.46430429_46430430insGTA NCBI36
NG_009205.2:g.33135_33136insTAC
NG_009205.3:g.33135_33136insTAC

Transcript Alleles

HGVS Amino-acid change
ENST00000396420.8:c.1466_1467insTAC (POMGNT1) ENSP00000379698.4:p.Glu489delinsAspThr
ENST00000477114.2:n.2028_2029insTAC (POMGNT1)
ENST00000497439.6:n.1638_1639insTAC (POMGNT1)
ENST00000684817.1:n.1826_1827insTAC (POMGNT1)
ENST00000684898.1:n.2028_2029insTAC (POMGNT1)
ENST00000685230.1:c.*776_*777insTAC (POMGNT1) ENSP00000510305.1:n.*776_*777insTAC
ENST00000685275.1:n.2013_2014insTAC (POMGNT1)
ENST00000685444.1:c.1367_1368insTAC (POMGNT1) ENSP00000510762.1:p.Glu456delinsAspThr
ENST00000685704.1:n.2028_2029insTAC (POMGNT1)
ENST00000685775.1:n.2993_2994insTAC (POMGNT1)
ENST00000685833.1:n.2344_2345insTAC (POMGNT1)
ENST00000686252.1:n.2540_2541insTAC (POMGNT1)
ENST00000686379.1:c.*590_*591insTAC (POMGNT1) ENSP00000508913.1:n.*590_*591insTAC
ENST00000686724.1:n.1638_1639insTAC (POMGNT1)
ENST00000686737.1:c.1466_1467insTAC (POMGNT1) ENSP00000508736.1:p.Glu489delinsAspThr
ENST00000687112.1:n.2332_2333insTAC (POMGNT1)
ENST00000687149.1:c.1466_1467insTAC (POMGNT1) ENSP00000509745.1:p.Glu489delinsAspThr
ENST00000687197.1:c.*406_*407insTAC (POMGNT1) ENSP00000510749.1:n.*406_*407insTAC
ENST00000687235.1:n.2028_2029insTAC (POMGNT1)
ENST00000687613.1:n.2216_2217insTAC (POMGNT1)
ENST00000687683.1:c.1466_1467insTAC (POMGNT1) ENSP00000508522.1:p.Glu489delinsAspThr
ENST00000688032.1:n.2028_2029insTAC (POMGNT1)
ENST00000688596.1:n.2117_2118insTAC (POMGNT1)
ENST00000688608.1:c.1367_1368insTAC (POMGNT1) ENSP00000508890.1:p.Glu456delinsAspThr
ENST00000688919.1:n.2662_2663insTAC (POMGNT1)
ENST00000689031.1:n.2028_2029insTAC (POMGNT1)
ENST00000689717.1:n.1638_1639insTAC (POMGNT1)
ENST00000689756.1:c.*1098_*1099insTAC (POMGNT1) ENSP00000509023.1:n.*1098_*1099insTAC
ENST00000690377.1:n.1813_1814insTAC (POMGNT1)
ENST00000690678.1:c.1466_1467insTAC (POMGNT1) ENSP00000508703.1:p.Glu489delinsAspThr
ENST00000691209.1:c.*406_*407insTAC (POMGNT1) ENSP00000510112.1:n.*406_*407insTAC
ENST00000691243.1:c.1466_1467insTAC (POMGNT1) ENSP00000510654.1:p.Glu489delinsAspThr
ENST00000692169.1:n.1615_1616insTAC (POMGNT1)
ENST00000692202.1:n.2041_2042insTAC (POMGNT1)
ENST00000692322.1:c.*1318_*1319insTAC (POMGNT1) ENSP00000509017.1:n.*1318_*1319insTAC
ENST00000692369.1:c.1466_1467insTAC (POMGNT1) ENSP00000508453.1:p.Glu489delinsAspThr
ENST00000692599.1:n.2028_2029insTAC (POMGNT1)
ENST00000692635.1:c.*406_*407insTAC (POMGNT1) ENSP00000508425.1:n.*406_*407insTAC
ENST00000693168.1:n.1727_1728insTAC (POMGNT1)
ENST00000693218.1:c.1466_1467insTAC (POMGNT1) ENSP00000510577.1:p.Glu489delinsAspThr
ENST00000693223.1:n.2414_2415insTAC (POMGNT1)
ENST00000693365.1:n.4100_4101insTAC (POMGNT1)
ENST00000371984.8:c.1466_1467insTAC (POMGNT1) MANE Select ENSP00000361052.3:p.Glu489delinsAspThr
ENST00000371984.7:c.1466_1467insTAC (POMGNT1) ENSP00000361052.3:p.Glu489delinsAspThr
ENST00000371992.1:c.1466_1467insTAC (POMGNT1) ENSP00000361060.1:p.Glu489delinsAspThr
ENST00000396420.7:c.*1135_*1136insTAC (POMGNT1) ENSP00000379698.3:n.*1135_*1136insTAC
ENST00000463030.1:n.87_88insTAC (POMGNT1)
ENST00000485714.1:n.852_853insTAC (POMGNT1)
NM_001243766.1:c.1466_1467insTAC (POMGNT1) NP_001230695.1:p.Glu489delinsAspThr
NM_001290129.1:c.1400_1401insTAC (POMGNT1) NP_001277058.1:p.Glu467delinsAspThr
NM_001290130.1:c.1037_1038insTAC (POMGNT1) NP_001277059.1:p.Glu346delinsAspThr
NM_017739.3:c.1466_1467insTAC (POMGNT1) NP_060209.3:p.Glu489delinsAspThr
XM_005271010.1:c.1466_1467insTAC (POMGNT1) XP_005271067.1:p.Glu489delinsAspThr
XM_006710755.1:c.1466_1467insTAC (POMGNT1) XP_006710818.1:p.Glu489delinsAspThr
XM_006710756.1:c.1466_1467insTAC (POMGNT1) XP_006710819.1:p.Glu489delinsAspThr
XM_011540460.1:c.679-4032_679-4031insGTA (TSPAN1) XP_011538762.1:n.679-4032_679-4031insGTA
XM_011540461.1:c.634-4032_634-4031insGTA (TSPAN1) XP_011538763.1:n.634-4032_634-4031insGTA
XM_011541759.1:c.1400_1401insTAC (POMGNT1) XP_011540061.1:p.Glu467delinsAspThr
XM_011541760.1:c.1400_1401insTAC (POMGNT1) XP_011540062.1:p.Glu467delinsAspThr
XM_011541761.1:c.374_375insTAC (POMGNT1) XP_011540063.1:p.Glu125delinsAspThr
XR_946706.1:n.1626_1627insTAC (POMGNT1)
XM_011540460.3:c.679-4032_679-4031insGTA (TSPAN1) XP_011538762.1:n.679-4032_679-4031insGTA
XM_011541760.3:c.1400_1401insTAC (POMGNT1) XP_011540062.1:p.Glu467delinsAspThr
XM_017001690.1:c.1466_1467insTAC (POMGNT1) XP_016857179.1:p.Glu489delinsAspThr
NM_001243766.2:c.1466_1467insTAC (POMGNT1) NP_001230695.2:p.Glu489delinsAspThr
NM_001290129.2:c.1400_1401insTAC (POMGNT1) NP_001277058.2:p.Glu467delinsAspThr
NM_001290130.2:c.1037_1038insTAC (POMGNT1) NP_001277059.2:p.Glu346delinsAspThr
NM_017739.4:c.1466_1467insTAC (POMGNT1) MANE Select NP_060209.4:p.Glu489delinsAspThr