Canonical Allele Identifier: CA340171210
Gene: POMGNT1 HGNC NCBI
TSPAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46189865G>T , CM000663.2:g.46189865G>T GRCh38
NC_000001.10:g.46655537G>T , CM000663.1:g.46655537G>T GRCh37
NC_000001.9:g.46428124G>T NCBI36
NG_009205.2:g.35441C>A
NG_009205.3:g.35441C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396420.8:c.1774C>A (POMGNT1) ENSP00000379698.4:p.Gln592Lys
ENST00000497439.6:n.1946C>A (POMGNT1)
ENST00000684817.1:n.2134C>A (POMGNT1)
ENST00000684898.1:n.2336C>A (POMGNT1)
ENST00000685230.1:c.*1084C>A (POMGNT1) ENSP00000510305.1:n.*1084C>A
ENST00000685275.1:n.2321C>A (POMGNT1)
ENST00000685444.1:c.1675C>A (POMGNT1) ENSP00000510762.1:p.Gln559Lys
ENST00000685704.1:n.2440C>A (POMGNT1)
ENST00000685833.1:n.4167C>A (POMGNT1)
ENST00000686252.1:n.2848C>A (POMGNT1)
ENST00000686379.1:c.*898C>A (POMGNT1) ENSP00000508913.1:n.*898C>A
ENST00000686724.1:n.3461C>A (POMGNT1)
ENST00000686737.1:c.1774C>A (POMGNT1) ENSP00000508736.1:p.Gln592Lys
ENST00000687112.1:n.2640C>A (POMGNT1)
ENST00000687149.1:c.1813C>A (POMGNT1) ENSP00000509745.1:p.Gln605Lys
ENST00000687197.1:c.*714C>A (POMGNT1) ENSP00000510749.1:n.*714C>A
ENST00000687235.1:n.3851C>A (POMGNT1)
ENST00000687613.1:n.2414C>A (POMGNT1)
ENST00000687683.1:c.1774C>A (POMGNT1) ENSP00000508522.1:p.Gln592Lys
ENST00000688032.1:n.2311C>A (POMGNT1)
ENST00000688596.1:n.2425C>A (POMGNT1)
ENST00000688608.1:c.1675C>A (POMGNT1) ENSP00000508890.1:p.Gln559Lys
ENST00000689031.1:n.2226C>A (POMGNT1)
ENST00000689756.1:c.*1406C>A (POMGNT1) ENSP00000509023.1:n.*1406C>A
ENST00000690377.1:n.2121C>A (POMGNT1)
ENST00000690678.1:c.1774C>A (POMGNT1) ENSP00000508703.1:p.Gln592Lys
ENST00000691209.1:c.*714C>A (POMGNT1) ENSP00000510112.1:n.*714C>A
ENST00000691243.1:c.*165C>A (POMGNT1) ENSP00000510654.1:n.*165C>A
ENST00000692202.1:n.2349C>A (POMGNT1)
ENST00000692322.1:c.*1561C>A (POMGNT1) ENSP00000509017.1:n.*1561C>A
ENST00000692369.1:c.1774C>A (POMGNT1) ENSP00000508453.1:p.Gln592Lys
ENST00000692599.1:n.3649C>A (POMGNT1)
ENST00000692635.1:c.*649C>A (POMGNT1) ENSP00000508425.1:n.*649C>A
ENST00000693168.1:n.3550C>A (POMGNT1)
ENST00000693218.1:c.*335C>A (POMGNT1) ENSP00000510577.1:n.*335C>A
ENST00000693223.1:n.2722C>A (POMGNT1)
ENST00000371984.8:c.1774C>A (POMGNT1) MANE Select ENSP00000361052.3:p.Gln592Lys
ENST00000371984.7:c.1774C>A (POMGNT1) ENSP00000361052.3:p.Gln592Lys
ENST00000371992.1:c.1774C>A (POMGNT1) ENSP00000361060.1:p.Gln592Lys
ENST00000396420.7:c.*1443C>A (POMGNT1) ENSP00000379698.3:n.*1443C>A
ENST00000480972.1:n.423C>A (POMGNT1)
NM_001243766.1:c.1774C>A (POMGNT1) NP_001230695.1:p.Gln592Lys
NM_001290129.1:c.1708C>A (POMGNT1) NP_001277058.1:p.Gln570Lys
NM_001290130.1:c.1345C>A (POMGNT1) NP_001277059.1:p.Gln449Lys
NM_017739.3:c.1774C>A (POMGNT1) NP_060209.3:p.Gln592Lys
XM_005271010.1:c.1774C>A (POMGNT1) XP_005271067.1:p.Gln592Lys
XM_006710755.1:c.1774C>A (POMGNT1) XP_006710818.1:p.Gln592Lys
XM_006710756.1:c.1774C>A (POMGNT1) XP_006710819.1:p.Gln592Lys
XM_011540460.1:c.678+4557G>T (TSPAN1) XP_011538762.1:n.678+4557G>T
XM_011540461.1:c.633+4557G>T (TSPAN1) XP_011538763.1:n.633+4557G>T
XM_011541759.1:c.1708C>A (POMGNT1) XP_011540061.1:p.Gln570Lys
XM_011541760.1:c.1708C>A (POMGNT1) XP_011540062.1:p.Gln570Lys
XM_011541761.1:c.682C>A (POMGNT1) XP_011540063.1:p.Gln228Lys
XM_011540460.3:c.678+4557G>T (TSPAN1) XP_011538762.1:n.678+4557G>T
XM_011541760.3:c.1708C>A (POMGNT1) XP_011540062.1:p.Gln570Lys
XM_017001690.1:c.1774C>A (POMGNT1) XP_016857179.1:p.Gln592Lys
NM_001243766.2:c.1774C>A (POMGNT1) NP_001230695.2:p.Gln592Lys
NM_001290129.2:c.1708C>A (POMGNT1) NP_001277058.2:p.Gln570Lys
NM_001290130.2:c.1345C>A (POMGNT1) NP_001277059.2:p.Gln449Lys
NM_017739.4:c.1774C>A (POMGNT1) MANE Select NP_060209.4:p.Gln592Lys