Canonical Allele Identifier: CA340171582

Gene: POMGNT1 TSPAN1

Linked Data

• MyVariant Identifiers: chr1:g.46655638C>G (hg19) ; chr1:g.46189966C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46189966C>G , CM000663.2:g.46189966C>G	GRCh38
NC_000001.10:g.46655638C>G , CM000663.1:g.46655638C>G	GRCh37
NC_000001.9:g.46428225C>G	NCBI36
NG_009205.2:g.35340G>C
NG_009205.3:g.35340G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396420.8:c.1673G>C (POMGNT1)	ENSP00000379698.4:p.Ser558Thr
ENST00000497439.6:n.1845G>C (POMGNT1)
ENST00000684817.1:n.2033G>C (POMGNT1)
ENST00000684898.1:n.2235G>C (POMGNT1)
ENST00000685230.1:c.*983G>C (POMGNT1)	ENSP00000510305.1:n.*983G>C
ENST00000685275.1:n.2220G>C (POMGNT1)
ENST00000685444.1:c.1574G>C (POMGNT1)	ENSP00000510762.1:p.Ser525Thr
ENST00000685704.1:n.2339G>C (POMGNT1)
ENST00000685833.1:n.4066G>C (POMGNT1)
ENST00000686252.1:n.2747G>C (POMGNT1)
ENST00000686379.1:c.*797G>C (POMGNT1)	ENSP00000508913.1:n.*797G>C
ENST00000686724.1:n.3360G>C (POMGNT1)
ENST00000686737.1:c.1673G>C (POMGNT1)	ENSP00000508736.1:p.Ser558Thr
ENST00000687112.1:n.2539G>C (POMGNT1)
ENST00000687149.1:c.1712G>C (POMGNT1)	ENSP00000509745.1:p.Ser571Thr
ENST00000687197.1:c.*613G>C (POMGNT1)	ENSP00000510749.1:n.*613G>C
ENST00000687235.1:n.3750G>C (POMGNT1)
ENST00000687613.1:n.2313G>C (POMGNT1)
ENST00000687683.1:c.1673G>C (POMGNT1)	ENSP00000508522.1:p.Ser558Thr
ENST00000688032.1:n.2210G>C (POMGNT1)
ENST00000688596.1:n.2324G>C (POMGNT1)
ENST00000688608.1:c.1574G>C (POMGNT1)	ENSP00000508890.1:p.Ser525Thr
ENST00000689031.1:n.2125G>C (POMGNT1)
ENST00000689756.1:c.*1305G>C (POMGNT1)	ENSP00000509023.1:n.*1305G>C
ENST00000690377.1:n.2020G>C (POMGNT1)
ENST00000690678.1:c.1673G>C (POMGNT1)	ENSP00000508703.1:p.Ser558Thr
ENST00000691209.1:c.*613G>C (POMGNT1)	ENSP00000510112.1:n.*613G>C
ENST00000691243.1:c.*64G>C (POMGNT1)	ENSP00000510654.1:n.*64G>C
ENST00000692202.1:n.2248G>C (POMGNT1)
ENST00000692322.1:c.*1460G>C (POMGNT1)	ENSP00000509017.1:n.*1460G>C
ENST00000692369.1:c.1673G>C (POMGNT1)	ENSP00000508453.1:p.Ser558Thr
ENST00000692599.1:n.3548G>C (POMGNT1)
ENST00000692635.1:c.*548G>C (POMGNT1)	ENSP00000508425.1:n.*548G>C
ENST00000693168.1:n.3449G>C (POMGNT1)
ENST00000693218.1:c.*234G>C (POMGNT1)	ENSP00000510577.1:n.*234G>C
ENST00000693223.1:n.2621G>C (POMGNT1)
ENST00000371984.8:c.1673G>C (POMGNT1) MANE Select	ENSP00000361052.3:p.Ser558Thr
ENST00000371984.7:c.1673G>C (POMGNT1)	ENSP00000361052.3:p.Ser558Thr
ENST00000371992.1:c.1673G>C (POMGNT1)	ENSP00000361060.1:p.Ser558Thr
ENST00000396420.7:c.*1342G>C (POMGNT1)	ENSP00000379698.3:n.*1342G>C
ENST00000480972.1:n.322G>C (POMGNT1)
NM_001243766.1:c.1673G>C (POMGNT1)	NP_001230695.1:p.Ser558Thr
NM_001290129.1:c.1607G>C (POMGNT1)	NP_001277058.1:p.Ser536Thr
NM_001290130.1:c.1244G>C (POMGNT1)	NP_001277059.1:p.Ser415Thr
NM_017739.3:c.1673G>C (POMGNT1)	NP_060209.3:p.Ser558Thr
XM_005271010.1:c.1673G>C (POMGNT1)	XP_005271067.1:p.Ser558Thr
XM_006710755.1:c.1673G>C (POMGNT1)	XP_006710818.1:p.Ser558Thr
XM_006710756.1:c.1673G>C (POMGNT1)	XP_006710819.1:p.Ser558Thr
XM_011540460.1:c.678+4658C>G (TSPAN1)	XP_011538762.1:n.678+4658C>G
XM_011540461.1:c.633+4658C>G (TSPAN1)	XP_011538763.1:n.633+4658C>G
XM_011541759.1:c.1607G>C (POMGNT1)	XP_011540061.1:p.Ser536Thr
XM_011541760.1:c.1607G>C (POMGNT1)	XP_011540062.1:p.Ser536Thr
XM_011541761.1:c.581G>C (POMGNT1)	XP_011540063.1:p.Ser194Thr
XM_011540460.3:c.678+4658C>G (TSPAN1)	XP_011538762.1:n.678+4658C>G
XM_011541760.3:c.1607G>C (POMGNT1)	XP_011540062.1:p.Ser536Thr
XM_017001690.1:c.1673G>C (POMGNT1)	XP_016857179.1:p.Ser558Thr
NM_001243766.2:c.1673G>C (POMGNT1)	NP_001230695.2:p.Ser558Thr
NM_001290129.2:c.1607G>C (POMGNT1)	NP_001277058.2:p.Ser536Thr
NM_001290130.2:c.1244G>C (POMGNT1)	NP_001277059.2:p.Ser415Thr
NM_017739.4:c.1673G>C (POMGNT1) MANE Select	NP_060209.4:p.Ser558Thr