Canonical Allele Identifier: CA2645441111
Gene: POMGNT1 HGNC NCBI
TSPAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46192168_46192172del , CM000663.2:g.46192168_46192172del GRCh38
NC_000001.10:g.46657840_46657844del , CM000663.1:g.46657840_46657844del GRCh37
NC_000001.9:g.46430427_46430431del NCBI36
NG_009205.2:g.33134_33138del
NG_009205.3:g.33134_33138del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396420.8:c.1465_1469del (POMGNT1) ENSP00000379698.4:p.Glu489HisfsTer4
ENST00000477114.2:n.2027_2031del (POMGNT1)
ENST00000497439.6:n.1637_1641del (POMGNT1)
ENST00000684817.1:n.1825_1829del (POMGNT1)
ENST00000684898.1:n.2027_2031del (POMGNT1)
ENST00000685230.1:c.*775_*779del (POMGNT1) ENSP00000510305.1:n.*775_*779del
ENST00000685275.1:n.2012_2016del (POMGNT1)
ENST00000685444.1:c.1366_1370del (POMGNT1) ENSP00000510762.1:p.Glu456HisfsTer4
ENST00000685704.1:n.2027_2031del (POMGNT1)
ENST00000685775.1:n.2992_2996del (POMGNT1)
ENST00000685833.1:n.2343_2347del (POMGNT1)
ENST00000686252.1:n.2539_2543del (POMGNT1)
ENST00000686379.1:c.*589_*593del (POMGNT1) ENSP00000508913.1:n.*589_*593del
ENST00000686724.1:n.1637_1641del (POMGNT1)
ENST00000686737.1:c.1465_1469del (POMGNT1) ENSP00000508736.1:p.Glu489HisfsTer4
ENST00000687112.1:n.2331_2335del (POMGNT1)
ENST00000687149.1:c.1465_1469del (POMGNT1) ENSP00000509745.1:p.Glu489HisfsTer4
ENST00000687197.1:c.*405_*409del (POMGNT1) ENSP00000510749.1:n.*405_*409del
ENST00000687235.1:n.2027_2031del (POMGNT1)
ENST00000687613.1:n.2215_2219del (POMGNT1)
ENST00000687683.1:c.1465_1469del (POMGNT1) ENSP00000508522.1:p.Glu489HisfsTer4
ENST00000688032.1:n.2027_2031del (POMGNT1)
ENST00000688596.1:n.2116_2120del (POMGNT1)
ENST00000688608.1:c.1366_1370del (POMGNT1) ENSP00000508890.1:p.Glu456HisfsTer4
ENST00000688919.1:n.2661_2665del (POMGNT1)
ENST00000689031.1:n.2027_2031del (POMGNT1)
ENST00000689717.1:n.1637_1641del (POMGNT1)
ENST00000689756.1:c.*1097_*1101del (POMGNT1) ENSP00000509023.1:n.*1097_*1101del
ENST00000690377.1:n.1812_1816del (POMGNT1)
ENST00000690678.1:c.1465_1469del (POMGNT1) ENSP00000508703.1:p.Glu489HisfsTer4
ENST00000691209.1:c.*405_*409del (POMGNT1) ENSP00000510112.1:n.*405_*409del
ENST00000691243.1:c.1465_1469del (POMGNT1) ENSP00000510654.1:p.Glu489HisfsTer4
ENST00000692169.1:n.1614_1618del (POMGNT1)
ENST00000692202.1:n.2040_2044del (POMGNT1)
ENST00000692322.1:c.*1317_*1321del (POMGNT1) ENSP00000509017.1:n.*1317_*1321del
ENST00000692369.1:c.1465_1469del (POMGNT1) ENSP00000508453.1:p.Glu489HisfsTer4
ENST00000692599.1:n.2027_2031del (POMGNT1)
ENST00000692635.1:c.*405_*409del (POMGNT1) ENSP00000508425.1:n.*405_*409del
ENST00000693168.1:n.1726_1730del (POMGNT1)
ENST00000693218.1:c.1465_1469del (POMGNT1) ENSP00000510577.1:p.Glu489HisfsTer4
ENST00000693223.1:n.2413_2417del (POMGNT1)
ENST00000693365.1:n.4099_4103del (POMGNT1)
ENST00000371984.8:c.1465_1469del (POMGNT1) MANE Select ENSP00000361052.3:p.Glu489HisfsTer4
ENST00000371984.7:c.1465_1469del (POMGNT1) ENSP00000361052.3:p.Glu489HisfsTer4
ENST00000371992.1:c.1465_1469del (POMGNT1) ENSP00000361060.1:p.Glu489HisfsTer4
ENST00000396420.7:c.*1134_*1138del (POMGNT1) ENSP00000379698.3:n.*1134_*1138del
ENST00000463030.1:n.86_90del (POMGNT1)
ENST00000485714.1:n.851_855del (POMGNT1)
NM_001243766.1:c.1465_1469del (POMGNT1) NP_001230695.1:p.Glu489HisfsTer4
NM_001290129.1:c.1399_1403del (POMGNT1) NP_001277058.1:p.Glu467HisfsTer4
NM_001290130.1:c.1036_1040del (POMGNT1) NP_001277059.1:p.Glu346HisfsTer4
NM_017739.3:c.1465_1469del (POMGNT1) NP_060209.3:p.Glu489HisfsTer4
XM_005271010.1:c.1465_1469del (POMGNT1) XP_005271067.1:p.Glu489HisfsTer4
XM_006710755.1:c.1465_1469del (POMGNT1) XP_006710818.1:p.Glu489HisfsTer4
XM_006710756.1:c.1465_1469del (POMGNT1) XP_006710819.1:p.Glu489HisfsTer4
XM_011540460.1:c.679-4034_679-4030del (TSPAN1) XP_011538762.1:n.679-4034_679-4030del
XM_011540461.1:c.634-4034_634-4030del (TSPAN1) XP_011538763.1:n.634-4034_634-4030del
XM_011541759.1:c.1399_1403del (POMGNT1) XP_011540061.1:p.Glu467HisfsTer4
XM_011541760.1:c.1399_1403del (POMGNT1) XP_011540062.1:p.Glu467HisfsTer4
XM_011541761.1:c.373_377del (POMGNT1) XP_011540063.1:p.Glu125HisfsTer4
XR_946706.1:n.1625_1629del (POMGNT1)
XM_011540460.3:c.679-4034_679-4030del (TSPAN1) XP_011538762.1:n.679-4034_679-4030del
XM_011541760.3:c.1399_1403del (POMGNT1) XP_011540062.1:p.Glu467HisfsTer4
XM_017001690.1:c.1465_1469del (POMGNT1) XP_016857179.1:p.Glu489HisfsTer4
NM_001243766.2:c.1465_1469del (POMGNT1) NP_001230695.2:p.Glu489HisfsTer4
NM_001290129.2:c.1399_1403del (POMGNT1) NP_001277058.2:p.Glu467HisfsTer4
NM_001290130.2:c.1036_1040del (POMGNT1) NP_001277059.2:p.Glu346HisfsTer4
NM_017739.4:c.1465_1469del (POMGNT1) MANE Select NP_060209.4:p.Glu489HisfsTer4