Canonical Allele Identifier: CA340171301
Gene: POMGNT1 HGNC NCBI
TSPAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46189887A>T , CM000663.2:g.46189887A>T GRCh38
NC_000001.10:g.46655559A>T , CM000663.1:g.46655559A>T GRCh37
NC_000001.9:g.46428146A>T NCBI36
NG_009205.2:g.35419T>A
NG_009205.3:g.35419T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396420.8:c.1752T>A (POMGNT1) ENSP00000379698.4:p.Asp584Glu
ENST00000497439.6:n.1924T>A (POMGNT1)
ENST00000684817.1:n.2112T>A (POMGNT1)
ENST00000684898.1:n.2314T>A (POMGNT1)
ENST00000685230.1:c.*1062T>A (POMGNT1) ENSP00000510305.1:n.*1062T>A
ENST00000685275.1:n.2299T>A (POMGNT1)
ENST00000685444.1:c.1653T>A (POMGNT1) ENSP00000510762.1:p.Asp551Glu
ENST00000685704.1:n.2418T>A (POMGNT1)
ENST00000685833.1:n.4145T>A (POMGNT1)
ENST00000686252.1:n.2826T>A (POMGNT1)
ENST00000686379.1:c.*876T>A (POMGNT1) ENSP00000508913.1:n.*876T>A
ENST00000686724.1:n.3439T>A (POMGNT1)
ENST00000686737.1:c.1752T>A (POMGNT1) ENSP00000508736.1:p.Asp584Glu
ENST00000687112.1:n.2618T>A (POMGNT1)
ENST00000687149.1:c.1791T>A (POMGNT1) ENSP00000509745.1:p.Asp597Glu
ENST00000687197.1:c.*692T>A (POMGNT1) ENSP00000510749.1:n.*692T>A
ENST00000687235.1:n.3829T>A (POMGNT1)
ENST00000687613.1:n.2392T>A (POMGNT1)
ENST00000687683.1:c.1752T>A (POMGNT1) ENSP00000508522.1:p.Asp584Glu
ENST00000688032.1:n.2289T>A (POMGNT1)
ENST00000688596.1:n.2403T>A (POMGNT1)
ENST00000688608.1:c.1653T>A (POMGNT1) ENSP00000508890.1:p.Asp551Glu
ENST00000689031.1:n.2204T>A (POMGNT1)
ENST00000689756.1:c.*1384T>A (POMGNT1) ENSP00000509023.1:n.*1384T>A
ENST00000690377.1:n.2099T>A (POMGNT1)
ENST00000690678.1:c.1752T>A (POMGNT1) ENSP00000508703.1:p.Asp584Glu
ENST00000691209.1:c.*692T>A (POMGNT1) ENSP00000510112.1:n.*692T>A
ENST00000691243.1:c.*143T>A (POMGNT1) ENSP00000510654.1:n.*143T>A
ENST00000692202.1:n.2327T>A (POMGNT1)
ENST00000692322.1:c.*1539T>A (POMGNT1) ENSP00000509017.1:n.*1539T>A
ENST00000692369.1:c.1752T>A (POMGNT1) ENSP00000508453.1:p.Asp584Glu
ENST00000692599.1:n.3627T>A (POMGNT1)
ENST00000692635.1:c.*627T>A (POMGNT1) ENSP00000508425.1:n.*627T>A
ENST00000693168.1:n.3528T>A (POMGNT1)
ENST00000693218.1:c.*313T>A (POMGNT1) ENSP00000510577.1:n.*313T>A
ENST00000693223.1:n.2700T>A (POMGNT1)
ENST00000371984.8:c.1752T>A (POMGNT1) MANE Select ENSP00000361052.3:p.Asp584Glu
ENST00000371984.7:c.1752T>A (POMGNT1) ENSP00000361052.3:p.Asp584Glu
ENST00000371992.1:c.1752T>A (POMGNT1) ENSP00000361060.1:p.Asp584Glu
ENST00000396420.7:c.*1421T>A (POMGNT1) ENSP00000379698.3:n.*1421T>A
ENST00000480972.1:n.401T>A (POMGNT1)
NM_001243766.1:c.1752T>A (POMGNT1) NP_001230695.1:p.Asp584Glu
NM_001290129.1:c.1686T>A (POMGNT1) NP_001277058.1:p.Asp562Glu
NM_001290130.1:c.1323T>A (POMGNT1) NP_001277059.1:p.Asp441Glu
NM_017739.3:c.1752T>A (POMGNT1) NP_060209.3:p.Asp584Glu
XM_005271010.1:c.1752T>A (POMGNT1) XP_005271067.1:p.Asp584Glu
XM_006710755.1:c.1752T>A (POMGNT1) XP_006710818.1:p.Asp584Glu
XM_006710756.1:c.1752T>A (POMGNT1) XP_006710819.1:p.Asp584Glu
XM_011540460.1:c.678+4579A>T (TSPAN1) XP_011538762.1:n.678+4579A>T
XM_011540461.1:c.633+4579A>T (TSPAN1) XP_011538763.1:n.633+4579A>T
XM_011541759.1:c.1686T>A (POMGNT1) XP_011540061.1:p.Asp562Glu
XM_011541760.1:c.1686T>A (POMGNT1) XP_011540062.1:p.Asp562Glu
XM_011541761.1:c.660T>A (POMGNT1) XP_011540063.1:p.Asp220Glu
XM_011540460.3:c.678+4579A>T (TSPAN1) XP_011538762.1:n.678+4579A>T
XM_011541760.3:c.1686T>A (POMGNT1) XP_011540062.1:p.Asp562Glu
XM_017001690.1:c.1752T>A (POMGNT1) XP_016857179.1:p.Asp584Glu
NM_001243766.2:c.1752T>A (POMGNT1) NP_001230695.2:p.Asp584Glu
NM_001290129.2:c.1686T>A (POMGNT1) NP_001277058.2:p.Asp562Glu
NM_001290130.2:c.1323T>A (POMGNT1) NP_001277059.2:p.Asp441Glu
NM_017739.4:c.1752T>A (POMGNT1) MANE Select NP_060209.4:p.Asp584Glu