Canonical Allele Identifier: CA340171244
Gene: POMGNT1 HGNC NCBI
TSPAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46189873G>T , CM000663.2:g.46189873G>T GRCh38
NC_000001.10:g.46655545G>T , CM000663.1:g.46655545G>T GRCh37
NC_000001.9:g.46428132G>T NCBI36
NG_009205.2:g.35433C>A
NG_009205.3:g.35433C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396420.8:c.1766C>A (POMGNT1) ENSP00000379698.4:p.Thr589Asn
ENST00000497439.6:n.1938C>A (POMGNT1)
ENST00000684817.1:n.2126C>A (POMGNT1)
ENST00000684898.1:n.2328C>A (POMGNT1)
ENST00000685230.1:c.*1076C>A (POMGNT1) ENSP00000510305.1:n.*1076C>A
ENST00000685275.1:n.2313C>A (POMGNT1)
ENST00000685444.1:c.1667C>A (POMGNT1) ENSP00000510762.1:p.Thr556Asn
ENST00000685704.1:n.2432C>A (POMGNT1)
ENST00000685833.1:n.4159C>A (POMGNT1)
ENST00000686252.1:n.2840C>A (POMGNT1)
ENST00000686379.1:c.*890C>A (POMGNT1) ENSP00000508913.1:n.*890C>A
ENST00000686724.1:n.3453C>A (POMGNT1)
ENST00000686737.1:c.1766C>A (POMGNT1) ENSP00000508736.1:p.Thr589Asn
ENST00000687112.1:n.2632C>A (POMGNT1)
ENST00000687149.1:c.1805C>A (POMGNT1) ENSP00000509745.1:p.Thr602Asn
ENST00000687197.1:c.*706C>A (POMGNT1) ENSP00000510749.1:n.*706C>A
ENST00000687235.1:n.3843C>A (POMGNT1)
ENST00000687613.1:n.2406C>A (POMGNT1)
ENST00000687683.1:c.1766C>A (POMGNT1) ENSP00000508522.1:p.Thr589Asn
ENST00000688032.1:n.2303C>A (POMGNT1)
ENST00000688596.1:n.2417C>A (POMGNT1)
ENST00000688608.1:c.1667C>A (POMGNT1) ENSP00000508890.1:p.Thr556Asn
ENST00000689031.1:n.2218C>A (POMGNT1)
ENST00000689756.1:c.*1398C>A (POMGNT1) ENSP00000509023.1:n.*1398C>A
ENST00000690377.1:n.2113C>A (POMGNT1)
ENST00000690678.1:c.1766C>A (POMGNT1) ENSP00000508703.1:p.Thr589Asn
ENST00000691209.1:c.*706C>A (POMGNT1) ENSP00000510112.1:n.*706C>A
ENST00000691243.1:c.*157C>A (POMGNT1) ENSP00000510654.1:n.*157C>A
ENST00000692202.1:n.2341C>A (POMGNT1)
ENST00000692322.1:c.*1553C>A (POMGNT1) ENSP00000509017.1:n.*1553C>A
ENST00000692369.1:c.1766C>A (POMGNT1) ENSP00000508453.1:p.Thr589Asn
ENST00000692599.1:n.3641C>A (POMGNT1)
ENST00000692635.1:c.*641C>A (POMGNT1) ENSP00000508425.1:n.*641C>A
ENST00000693168.1:n.3542C>A (POMGNT1)
ENST00000693218.1:c.*327C>A (POMGNT1) ENSP00000510577.1:n.*327C>A
ENST00000693223.1:n.2714C>A (POMGNT1)
ENST00000371984.8:c.1766C>A (POMGNT1) MANE Select ENSP00000361052.3:p.Thr589Asn
ENST00000371984.7:c.1766C>A (POMGNT1) ENSP00000361052.3:p.Thr589Asn
ENST00000371992.1:c.1766C>A (POMGNT1) ENSP00000361060.1:p.Thr589Asn
ENST00000396420.7:c.*1435C>A (POMGNT1) ENSP00000379698.3:n.*1435C>A
ENST00000480972.1:n.415C>A (POMGNT1)
NM_001243766.1:c.1766C>A (POMGNT1) NP_001230695.1:p.Thr589Asn
NM_001290129.1:c.1700C>A (POMGNT1) NP_001277058.1:p.Thr567Asn
NM_001290130.1:c.1337C>A (POMGNT1) NP_001277059.1:p.Thr446Asn
NM_017739.3:c.1766C>A (POMGNT1) NP_060209.3:p.Thr589Asn
XM_005271010.1:c.1766C>A (POMGNT1) XP_005271067.1:p.Thr589Asn
XM_006710755.1:c.1766C>A (POMGNT1) XP_006710818.1:p.Thr589Asn
XM_006710756.1:c.1766C>A (POMGNT1) XP_006710819.1:p.Thr589Asn
XM_011540460.1:c.678+4565G>T (TSPAN1) XP_011538762.1:n.678+4565G>T
XM_011540461.1:c.633+4565G>T (TSPAN1) XP_011538763.1:n.633+4565G>T
XM_011541759.1:c.1700C>A (POMGNT1) XP_011540061.1:p.Thr567Asn
XM_011541760.1:c.1700C>A (POMGNT1) XP_011540062.1:p.Thr567Asn
XM_011541761.1:c.674C>A (POMGNT1) XP_011540063.1:p.Thr225Asn
XM_011540460.3:c.678+4565G>T (TSPAN1) XP_011538762.1:n.678+4565G>T
XM_011541760.3:c.1700C>A (POMGNT1) XP_011540062.1:p.Thr567Asn
XM_017001690.1:c.1766C>A (POMGNT1) XP_016857179.1:p.Thr589Asn
NM_001243766.2:c.1766C>A (POMGNT1) NP_001230695.2:p.Thr589Asn
NM_001290129.2:c.1700C>A (POMGNT1) NP_001277058.2:p.Thr567Asn
NM_001290130.2:c.1337C>A (POMGNT1) NP_001277059.2:p.Thr446Asn
NM_017739.4:c.1766C>A (POMGNT1) MANE Select NP_060209.4:p.Thr589Asn