Canonical Allele Identifier: CA417886254

Gene: POMGNT1 TSPAN1

Linked Data

• MyVariant Identifiers: chr1:g.46658079T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46192407T>G , CM000663.2:g.46192407T>G	GRCh38
NC_000001.10:g.46658079T>G , CM000663.1:g.46658079T>G	GRCh37
NC_000001.9:g.46430666T>G	NCBI36
NG_009205.2:g.32899A>C
NG_009205.3:g.32899A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396420.8:c.1314A>C (POMGNT1)	ENSP00000379698.4:p.Ala438=
ENST00000477114.2:n.1876A>C (POMGNT1)
ENST00000497439.6:n.1486A>C (POMGNT1)
ENST00000684817.1:n.1674A>C (POMGNT1)
ENST00000684898.1:n.1876A>C (POMGNT1)
ENST00000685230.1:c.*624A>C (POMGNT1)	ENSP00000510305.1:n.*624A>C
ENST00000685275.1:n.1861A>C (POMGNT1)
ENST00000685444.1:c.1215A>C (POMGNT1)	ENSP00000510762.1:p.Ala405=
ENST00000685704.1:n.1876A>C (POMGNT1)
ENST00000685775.1:n.2841A>C (POMGNT1)
ENST00000685833.1:n.2192A>C (POMGNT1)
ENST00000686252.1:n.2388A>C (POMGNT1)
ENST00000686379.1:c.*438A>C (POMGNT1)	ENSP00000508913.1:n.*438A>C
ENST00000686724.1:n.1486A>C (POMGNT1)
ENST00000686737.1:c.1314A>C (POMGNT1)	ENSP00000508736.1:p.Ala438=
ENST00000687112.1:n.2180A>C (POMGNT1)
ENST00000687149.1:c.1314A>C (POMGNT1)	ENSP00000509745.1:p.Ala438=
ENST00000687197.1:c.*254A>C (POMGNT1)	ENSP00000510749.1:n.*254A>C
ENST00000687235.1:n.1876A>C (POMGNT1)
ENST00000687613.1:n.2064A>C (POMGNT1)
ENST00000687683.1:c.1314A>C (POMGNT1)	ENSP00000508522.1:p.Ala438=
ENST00000688032.1:n.1876A>C (POMGNT1)
ENST00000688596.1:n.1965A>C (POMGNT1)
ENST00000688608.1:c.1215A>C (POMGNT1)	ENSP00000508890.1:p.Ala405=
ENST00000688919.1:n.2510A>C (POMGNT1)
ENST00000689031.1:n.1876A>C (POMGNT1)
ENST00000689717.1:n.1486A>C (POMGNT1)
ENST00000689756.1:c.*946A>C (POMGNT1)	ENSP00000509023.1:n.*946A>C
ENST00000690377.1:n.1661A>C (POMGNT1)
ENST00000690678.1:c.1314A>C (POMGNT1)	ENSP00000508703.1:p.Ala438=
ENST00000691209.1:c.*254A>C (POMGNT1)	ENSP00000510112.1:n.*254A>C
ENST00000691243.1:c.1314A>C (POMGNT1)	ENSP00000510654.1:p.Ala438=
ENST00000692169.1:n.1463A>C (POMGNT1)
ENST00000692202.1:n.1889A>C (POMGNT1)
ENST00000692322.1:c.*1166A>C (POMGNT1)	ENSP00000509017.1:n.*1166A>C
ENST00000692369.1:c.1314A>C (POMGNT1)	ENSP00000508453.1:p.Ala438=
ENST00000692599.1:n.1876A>C (POMGNT1)
ENST00000692635.1:c.*254A>C (POMGNT1)	ENSP00000508425.1:n.*254A>C
ENST00000693168.1:n.1575A>C (POMGNT1)
ENST00000693218.1:c.1314A>C (POMGNT1)	ENSP00000510577.1:p.Ala438=
ENST00000693223.1:n.2262A>C (POMGNT1)
ENST00000693365.1:n.3948A>C (POMGNT1)
ENST00000371984.8:c.1314A>C (POMGNT1) MANE Select	ENSP00000361052.3:p.Ala438=
ENST00000371984.7:c.1314A>C (POMGNT1)	ENSP00000361052.3:p.Ala438=
ENST00000371992.1:c.1314A>C (POMGNT1)	ENSP00000361060.1:p.Ala438=
ENST00000396420.7:c.*983A>C (POMGNT1)	ENSP00000379698.3:n.*983A>C
ENST00000485714.1:n.700A>C (POMGNT1)
NM_001243766.1:c.1314A>C (POMGNT1)	NP_001230695.1:p.Ala438=
NM_001290129.1:c.1248A>C (POMGNT1)	NP_001277058.1:p.Ala416=
NM_001290130.1:c.885A>C (POMGNT1)	NP_001277059.1:p.Ala295=
NM_017739.3:c.1314A>C (POMGNT1)	NP_060209.3:p.Ala438=
XM_005271010.1:c.1314A>C (POMGNT1)	XP_005271067.1:p.Ala438=
XM_006710755.1:c.1314A>C (POMGNT1)	XP_006710818.1:p.Ala438=
XM_006710756.1:c.1314A>C (POMGNT1)	XP_006710819.1:p.Ala438=
XM_011540460.1:c.679-3795T>G (TSPAN1)	XP_011538762.1:n.679-3795T>G
XM_011540461.1:c.634-3795T>G (TSPAN1)	XP_011538763.1:n.634-3795T>G
XM_011541759.1:c.1248A>C (POMGNT1)	XP_011540061.1:p.Ala416=
XM_011541760.1:c.1248A>C (POMGNT1)	XP_011540062.1:p.Ala416=
XM_011541761.1:c.222A>C (POMGNT1)	XP_011540063.1:p.Ala74=
XR_946706.1:n.1474A>C (POMGNT1)
XM_011540460.3:c.679-3795T>G (TSPAN1)	XP_011538762.1:n.679-3795T>G
XM_011541760.3:c.1248A>C (POMGNT1)	XP_011540062.1:p.Ala416=
XM_017001690.1:c.1314A>C (POMGNT1)	XP_016857179.1:p.Ala438=
NM_001243766.2:c.1314A>C (POMGNT1)	NP_001230695.2:p.Ala438=
NM_001290129.2:c.1248A>C (POMGNT1)	NP_001277058.2:p.Ala416=
NM_001290130.2:c.885A>C (POMGNT1)	NP_001277059.2:p.Ala295=
NM_017739.4:c.1314A>C (POMGNT1) MANE Select	NP_060209.4:p.Ala438=