Canonical Allele Identifier: CA340171762
Gene: POMGNT1 HGNC NCBI
TSPAN1 HGNC NCBI

Linked Data

dbSNP Id: rs1188550112

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46190479A>G , CM000663.2:g.46190479A>G GRCh38
NC_000001.10:g.46656151A>G , CM000663.1:g.46656151A>G GRCh37
NC_000001.9:g.46428738A>G NCBI36
NG_009205.2:g.34827T>C
NG_009205.3:g.34827T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000396420.8:c.1643T>C (POMGNT1) ENSP00000379698.4:p.Leu548Pro
ENST00000477114.2:n.2205T>C (POMGNT1)
ENST00000497439.6:n.1815T>C (POMGNT1)
ENST00000684817.1:n.2003T>C (POMGNT1)
ENST00000684898.1:n.2205T>C (POMGNT1)
ENST00000685230.1:c.*953T>C (POMGNT1) ENSP00000510305.1:n.*953T>C
ENST00000685275.1:n.2190T>C (POMGNT1)
ENST00000685444.1:c.1544T>C (POMGNT1) ENSP00000510762.1:p.Leu515Pro
ENST00000685704.1:n.2309T>C (POMGNT1)
ENST00000685775.1:n.4685T>C (POMGNT1)
ENST00000685833.1:n.4036T>C (POMGNT1)
ENST00000686252.1:n.2717T>C (POMGNT1)
ENST00000686379.1:c.*767T>C (POMGNT1) ENSP00000508913.1:n.*767T>C
ENST00000686724.1:n.3330T>C (POMGNT1)
ENST00000686737.1:c.1643T>C (POMGNT1) ENSP00000508736.1:p.Leu548Pro
ENST00000687112.1:n.2509T>C (POMGNT1)
ENST00000687149.1:c.1682T>C (POMGNT1) ENSP00000509745.1:p.Leu561Pro
ENST00000687197.1:c.*583T>C (POMGNT1) ENSP00000510749.1:n.*583T>C
ENST00000687235.1:n.3720T>C (POMGNT1)
ENST00000687613.1:n.2290-490T>C (POMGNT1)
ENST00000687683.1:c.1643T>C (POMGNT1) ENSP00000508522.1:p.Leu548Pro
ENST00000688032.1:n.2180T>C (POMGNT1)
ENST00000688596.1:n.2294T>C (POMGNT1)
ENST00000688608.1:c.1544T>C (POMGNT1) ENSP00000508890.1:p.Leu515Pro
ENST00000688919.1:n.3041T>C (POMGNT1)
ENST00000689031.1:n.2102-490T>C (POMGNT1)
ENST00000689717.1:n.2017T>C (POMGNT1)
ENST00000689756.1:c.*1275T>C (POMGNT1) ENSP00000509023.1:n.*1275T>C
ENST00000690377.1:n.1990T>C (POMGNT1)
ENST00000690678.1:c.1643T>C (POMGNT1) ENSP00000508703.1:p.Leu548Pro
ENST00000691209.1:c.*583T>C (POMGNT1) ENSP00000510112.1:n.*583T>C
ENST00000691243.1:c.*34T>C (POMGNT1) ENSP00000510654.1:n.*34T>C
ENST00000692169.1:n.3307T>C (POMGNT1)
ENST00000692202.1:n.2218T>C (POMGNT1)
ENST00000692322.1:c.*1430T>C (POMGNT1) ENSP00000509017.1:n.*1430T>C
ENST00000692369.1:c.1643T>C (POMGNT1) ENSP00000508453.1:p.Leu548Pro
ENST00000692599.1:n.3518T>C (POMGNT1)
ENST00000692635.1:c.*518T>C (POMGNT1) ENSP00000508425.1:n.*518T>C
ENST00000693168.1:n.3419T>C (POMGNT1)
ENST00000693218.1:c.*204T>C (POMGNT1) ENSP00000510577.1:n.*204T>C
ENST00000693223.1:n.2591T>C (POMGNT1)
ENST00000693365.1:n.5792T>C (POMGNT1)
ENST00000371984.8:c.1643T>C (POMGNT1) MANE Select ENSP00000361052.3:p.Leu548Pro
ENST00000371984.7:c.1643T>C (POMGNT1) ENSP00000361052.3:p.Leu548Pro
ENST00000371992.1:c.1643T>C (POMGNT1) ENSP00000361060.1:p.Leu548Pro
ENST00000396420.7:c.*1312T>C (POMGNT1) ENSP00000379698.3:n.*1312T>C
ENST00000480972.1:n.292T>C (POMGNT1)
ENST00000485714.1:n.2544T>C (POMGNT1)
NM_001243766.1:c.1643T>C (POMGNT1) NP_001230695.1:p.Leu548Pro
NM_001290129.1:c.1577T>C (POMGNT1) NP_001277058.1:p.Leu526Pro
NM_001290130.1:c.1214T>C (POMGNT1) NP_001277059.1:p.Leu405Pro
NM_017739.3:c.1643T>C (POMGNT1) NP_060209.3:p.Leu548Pro
XM_005271010.1:c.1643T>C (POMGNT1) XP_005271067.1:p.Leu548Pro
XM_006710755.1:c.1643T>C (POMGNT1) XP_006710818.1:p.Leu548Pro
XM_006710756.1:c.1643T>C (POMGNT1) XP_006710819.1:p.Leu548Pro
XM_011540460.1:c.678+5171A>G (TSPAN1) XP_011538762.1:n.678+5171A>G
XM_011540461.1:c.633+5171A>G (TSPAN1) XP_011538763.1:n.633+5171A>G
XM_011541759.1:c.1577T>C (POMGNT1) XP_011540061.1:p.Leu526Pro
XM_011541760.1:c.1577T>C (POMGNT1) XP_011540062.1:p.Leu526Pro
XM_011541761.1:c.551T>C (POMGNT1) XP_011540063.1:p.Leu184Pro
XM_011540460.3:c.678+5171A>G (TSPAN1) XP_011538762.1:n.678+5171A>G
XM_011541760.3:c.1577T>C (POMGNT1) XP_011540062.1:p.Leu526Pro
XM_017001690.1:c.1643T>C (POMGNT1) XP_016857179.1:p.Leu548Pro
NM_001243766.2:c.1643T>C (POMGNT1) NP_001230695.2:p.Leu548Pro
NM_001290129.2:c.1577T>C (POMGNT1) NP_001277058.2:p.Leu526Pro
NM_001290130.2:c.1214T>C (POMGNT1) NP_001277059.2:p.Leu405Pro
NM_017739.4:c.1643T>C (POMGNT1) MANE Select NP_060209.4:p.Leu548Pro