Canonical Allele Identifier: CA340176951
Gene: POMGNT1 HGNC NCBI
TSPAN1 HGNC NCBI

Linked Data

gnomAD v4: 1-46192579-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46192579T>C , CM000663.2:g.46192579T>C GRCh38
NC_000001.10:g.46658251T>C , CM000663.1:g.46658251T>C GRCh37
NC_000001.9:g.46430838T>C NCBI36
NG_009205.2:g.32727A>G
NG_009205.3:g.32727A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000396420.8:c.1223A>G (POMGNT1) ENSP00000379698.4:p.Gln408Arg
ENST00000477114.2:n.1785A>G (POMGNT1)
ENST00000497439.6:n.1395A>G (POMGNT1)
ENST00000684817.1:n.1583A>G (POMGNT1)
ENST00000684898.1:n.1785A>G (POMGNT1)
ENST00000685230.1:c.*533A>G (POMGNT1) ENSP00000510305.1:n.*533A>G
ENST00000685275.1:n.1770A>G (POMGNT1)
ENST00000685444.1:c.1124A>G (POMGNT1) ENSP00000510762.1:p.Gln375Arg
ENST00000685704.1:n.1785A>G (POMGNT1)
ENST00000685775.1:n.2750A>G (POMGNT1)
ENST00000685833.1:n.2101A>G (POMGNT1)
ENST00000686252.1:n.2297A>G (POMGNT1)
ENST00000686379.1:c.*347A>G (POMGNT1) ENSP00000508913.1:n.*347A>G
ENST00000686724.1:n.1395A>G (POMGNT1)
ENST00000686737.1:c.1223A>G (POMGNT1) ENSP00000508736.1:p.Gln408Arg
ENST00000687112.1:n.2089A>G (POMGNT1)
ENST00000687149.1:c.1223A>G (POMGNT1) ENSP00000509745.1:p.Gln408Arg
ENST00000687197.1:c.*163A>G (POMGNT1) ENSP00000510749.1:n.*163A>G
ENST00000687235.1:n.1785A>G (POMGNT1)
ENST00000687613.1:n.1973A>G (POMGNT1)
ENST00000687683.1:c.1223A>G (POMGNT1) ENSP00000508522.1:p.Gln408Arg
ENST00000688032.1:n.1785A>G (POMGNT1)
ENST00000688596.1:n.1874A>G (POMGNT1)
ENST00000688608.1:c.1124A>G (POMGNT1) ENSP00000508890.1:p.Gln375Arg
ENST00000688919.1:n.2419A>G (POMGNT1)
ENST00000689031.1:n.1785A>G (POMGNT1)
ENST00000689717.1:n.1395A>G (POMGNT1)
ENST00000689756.1:c.*855A>G (POMGNT1) ENSP00000509023.1:n.*855A>G
ENST00000690377.1:n.1570A>G (POMGNT1)
ENST00000690678.1:c.1223A>G (POMGNT1) ENSP00000508703.1:p.Gln408Arg
ENST00000691209.1:c.*163A>G (POMGNT1) ENSP00000510112.1:n.*163A>G
ENST00000691243.1:c.1223A>G (POMGNT1) ENSP00000510654.1:p.Gln408Arg
ENST00000692169.1:n.1372A>G (POMGNT1)
ENST00000692202.1:n.1798A>G (POMGNT1)
ENST00000692322.1:c.*1075A>G (POMGNT1) ENSP00000509017.1:n.*1075A>G
ENST00000692369.1:c.1223A>G (POMGNT1) ENSP00000508453.1:p.Gln408Arg
ENST00000692599.1:n.1785A>G (POMGNT1)
ENST00000692635.1:c.*163A>G (POMGNT1) ENSP00000508425.1:n.*163A>G
ENST00000693168.1:n.1484A>G (POMGNT1)
ENST00000693218.1:c.1223A>G (POMGNT1) ENSP00000510577.1:p.Gln408Arg
ENST00000693223.1:n.2171A>G (POMGNT1)
ENST00000693365.1:n.3857A>G (POMGNT1)
ENST00000371984.8:c.1223A>G (POMGNT1) MANE Select ENSP00000361052.3:p.Gln408Arg
ENST00000371984.7:c.1223A>G (POMGNT1) ENSP00000361052.3:p.Gln408Arg
ENST00000371992.1:c.1223A>G (POMGNT1) ENSP00000361060.1:p.Gln408Arg
ENST00000396420.7:c.*892A>G (POMGNT1) ENSP00000379698.3:n.*892A>G
ENST00000485714.1:n.609A>G (POMGNT1)
NM_001243766.1:c.1223A>G (POMGNT1) NP_001230695.1:p.Gln408Arg
NM_001290129.1:c.1157A>G (POMGNT1) NP_001277058.1:p.Gln386Arg
NM_001290130.1:c.794A>G (POMGNT1) NP_001277059.1:p.Gln265Arg
NM_017739.3:c.1223A>G (POMGNT1) NP_060209.3:p.Gln408Arg
XM_005271010.1:c.1223A>G (POMGNT1) XP_005271067.1:p.Gln408Arg
XM_006710755.1:c.1223A>G (POMGNT1) XP_006710818.1:p.Gln408Arg
XM_006710756.1:c.1223A>G (POMGNT1) XP_006710819.1:p.Gln408Arg
XM_011540460.1:c.679-3623T>C (TSPAN1) XP_011538762.1:n.679-3623T>C
XM_011540461.1:c.634-3623T>C (TSPAN1) XP_011538763.1:n.634-3623T>C
XM_011541759.1:c.1157A>G (POMGNT1) XP_011540061.1:p.Gln386Arg
XM_011541760.1:c.1157A>G (POMGNT1) XP_011540062.1:p.Gln386Arg
XM_011541761.1:c.131A>G (POMGNT1) XP_011540063.1:p.Gln44Arg
XR_946706.1:n.1383A>G (POMGNT1)
XM_011540460.3:c.679-3623T>C (TSPAN1) XP_011538762.1:n.679-3623T>C
XM_011541760.3:c.1157A>G (POMGNT1) XP_011540062.1:p.Gln386Arg
XM_017001690.1:c.1223A>G (POMGNT1) XP_016857179.1:p.Gln408Arg
NM_001243766.2:c.1223A>G (POMGNT1) NP_001230695.2:p.Gln408Arg
NM_001290129.2:c.1157A>G (POMGNT1) NP_001277058.2:p.Gln386Arg
NM_001290130.2:c.794A>G (POMGNT1) NP_001277059.2:p.Gln265Arg
NM_017739.4:c.1223A>G (POMGNT1) MANE Select NP_060209.4:p.Gln408Arg