Canonical Allele Identifier: CA340171737

Gene: POMGNT1 TSPAN1

Linked Data

• MyVariant Identifiers: chr1:g.46656145C>G (hg19) ; chr1:g.46190473C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46190473C>G , CM000663.2:g.46190473C>G	GRCh38
NC_000001.10:g.46656145C>G , CM000663.1:g.46656145C>G	GRCh37
NC_000001.9:g.46428732C>G	NCBI36
NG_009205.2:g.34833G>C
NG_009205.3:g.34833G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396420.8:c.1649G>C (POMGNT1)	ENSP00000379698.4:p.Ser550Thr
ENST00000477114.2:n.2211G>C (POMGNT1)
ENST00000497439.6:n.1821G>C (POMGNT1)
ENST00000684817.1:n.2009G>C (POMGNT1)
ENST00000684898.1:n.2211G>C (POMGNT1)
ENST00000685230.1:c.*959G>C (POMGNT1)	ENSP00000510305.1:n.*959G>C
ENST00000685275.1:n.2196G>C (POMGNT1)
ENST00000685444.1:c.1550G>C (POMGNT1)	ENSP00000510762.1:p.Ser517Thr
ENST00000685704.1:n.2315G>C (POMGNT1)
ENST00000685775.1:n.4691G>C (POMGNT1)
ENST00000685833.1:n.4042G>C (POMGNT1)
ENST00000686252.1:n.2723G>C (POMGNT1)
ENST00000686379.1:c.*773G>C (POMGNT1)	ENSP00000508913.1:n.*773G>C
ENST00000686724.1:n.3336G>C (POMGNT1)
ENST00000686737.1:c.1649G>C (POMGNT1)	ENSP00000508736.1:p.Ser550Thr
ENST00000687112.1:n.2515G>C (POMGNT1)
ENST00000687149.1:c.1688G>C (POMGNT1)	ENSP00000509745.1:p.Ser563Thr
ENST00000687197.1:c.*589G>C (POMGNT1)	ENSP00000510749.1:n.*589G>C
ENST00000687235.1:n.3726G>C (POMGNT1)
ENST00000687613.1:n.2290-484G>C (POMGNT1)
ENST00000687683.1:c.1649G>C (POMGNT1)	ENSP00000508522.1:p.Ser550Thr
ENST00000688032.1:n.2186G>C (POMGNT1)
ENST00000688596.1:n.2300G>C (POMGNT1)
ENST00000688608.1:c.1550G>C (POMGNT1)	ENSP00000508890.1:p.Ser517Thr
ENST00000688919.1:n.3047G>C (POMGNT1)
ENST00000689031.1:n.2102-484G>C (POMGNT1)
ENST00000689717.1:n.2023G>C (POMGNT1)
ENST00000689756.1:c.*1281G>C (POMGNT1)	ENSP00000509023.1:n.*1281G>C
ENST00000690377.1:n.1996G>C (POMGNT1)
ENST00000690678.1:c.1649G>C (POMGNT1)	ENSP00000508703.1:p.Ser550Thr
ENST00000691209.1:c.*589G>C (POMGNT1)	ENSP00000510112.1:n.*589G>C
ENST00000691243.1:c.*40G>C (POMGNT1)	ENSP00000510654.1:n.*40G>C
ENST00000692169.1:n.3313G>C (POMGNT1)
ENST00000692202.1:n.2224G>C (POMGNT1)
ENST00000692322.1:c.*1436G>C (POMGNT1)	ENSP00000509017.1:n.*1436G>C
ENST00000692369.1:c.1649G>C (POMGNT1)	ENSP00000508453.1:p.Ser550Thr
ENST00000692599.1:n.3524G>C (POMGNT1)
ENST00000692635.1:c.*524G>C (POMGNT1)	ENSP00000508425.1:n.*524G>C
ENST00000693168.1:n.3425G>C (POMGNT1)
ENST00000693218.1:c.*210G>C (POMGNT1)	ENSP00000510577.1:n.*210G>C
ENST00000693223.1:n.2597G>C (POMGNT1)
ENST00000693365.1:n.5798G>C (POMGNT1)
ENST00000371984.8:c.1649G>C (POMGNT1) MANE Select	ENSP00000361052.3:p.Ser550Thr
ENST00000371984.7:c.1649G>C (POMGNT1)	ENSP00000361052.3:p.Ser550Thr
ENST00000371992.1:c.1649G>C (POMGNT1)	ENSP00000361060.1:p.Ser550Thr
ENST00000396420.7:c.*1318G>C (POMGNT1)	ENSP00000379698.3:n.*1318G>C
ENST00000480972.1:n.298G>C (POMGNT1)
ENST00000485714.1:n.2550G>C (POMGNT1)
NM_001243766.1:c.1649G>C (POMGNT1)	NP_001230695.1:p.Ser550Thr
NM_001290129.1:c.1583G>C (POMGNT1)	NP_001277058.1:p.Ser528Thr
NM_001290130.1:c.1220G>C (POMGNT1)	NP_001277059.1:p.Ser407Thr
NM_017739.3:c.1649G>C (POMGNT1)	NP_060209.3:p.Ser550Thr
XM_005271010.1:c.1649G>C (POMGNT1)	XP_005271067.1:p.Ser550Thr
XM_006710755.1:c.1649G>C (POMGNT1)	XP_006710818.1:p.Ser550Thr
XM_006710756.1:c.1649G>C (POMGNT1)	XP_006710819.1:p.Ser550Thr
XM_011540460.1:c.678+5165C>G (TSPAN1)	XP_011538762.1:n.678+5165C>G
XM_011540461.1:c.633+5165C>G (TSPAN1)	XP_011538763.1:n.633+5165C>G
XM_011541759.1:c.1583G>C (POMGNT1)	XP_011540061.1:p.Ser528Thr
XM_011541760.1:c.1583G>C (POMGNT1)	XP_011540062.1:p.Ser528Thr
XM_011541761.1:c.557G>C (POMGNT1)	XP_011540063.1:p.Ser186Thr
XM_011540460.3:c.678+5165C>G (TSPAN1)	XP_011538762.1:n.678+5165C>G
XM_011541760.3:c.1583G>C (POMGNT1)	XP_011540062.1:p.Ser528Thr
XM_017001690.1:c.1649G>C (POMGNT1)	XP_016857179.1:p.Ser550Thr
NM_001243766.2:c.1649G>C (POMGNT1)	NP_001230695.2:p.Ser550Thr
NM_001290129.2:c.1583G>C (POMGNT1)	NP_001277058.2:p.Ser528Thr
NM_001290130.2:c.1220G>C (POMGNT1)	NP_001277059.2:p.Ser407Thr
NM_017739.4:c.1649G>C (POMGNT1) MANE Select	NP_060209.4:p.Ser550Thr