Canonical Allele Identifier: CA340174458

Gene: POMGNT1 TSPAN1

Linked Data

• dbSNP Id: rs1280404506
• gnomAD v2: 1-46657891-C-T
• gnomAD v4: 1-46192219-C-T
• MyVariant Identifiers: chr1:g.46657891C>T (hg19) ; chr1:g.46192219C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46192219C>T , CM000663.2:g.46192219C>T	GRCh38
NC_000001.10:g.46657891C>T , CM000663.1:g.46657891C>T	GRCh37
NC_000001.9:g.46430478C>T	NCBI36
NG_009205.2:g.33087G>A
NG_009205.3:g.33087G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396420.8:c.1418G>A (POMGNT1)	ENSP00000379698.4:p.Trp473Ter
ENST00000477114.2:n.1980G>A (POMGNT1)
ENST00000497439.6:n.1590G>A (POMGNT1)
ENST00000684817.1:n.1778G>A (POMGNT1)
ENST00000684898.1:n.1980G>A (POMGNT1)
ENST00000685230.1:c.*728G>A (POMGNT1)	ENSP00000510305.1:n.*728G>A
ENST00000685275.1:n.1965G>A (POMGNT1)
ENST00000685444.1:c.1319G>A (POMGNT1)	ENSP00000510762.1:p.Trp440Ter
ENST00000685704.1:n.1980G>A (POMGNT1)
ENST00000685775.1:n.2945G>A (POMGNT1)
ENST00000685833.1:n.2296G>A (POMGNT1)
ENST00000686252.1:n.2492G>A (POMGNT1)
ENST00000686379.1:c.*542G>A (POMGNT1)	ENSP00000508913.1:n.*542G>A
ENST00000686724.1:n.1590G>A (POMGNT1)
ENST00000686737.1:c.1418G>A (POMGNT1)	ENSP00000508736.1:p.Trp473Ter
ENST00000687112.1:n.2284G>A (POMGNT1)
ENST00000687149.1:c.1418G>A (POMGNT1)	ENSP00000509745.1:p.Trp473Ter
ENST00000687197.1:c.*358G>A (POMGNT1)	ENSP00000510749.1:n.*358G>A
ENST00000687235.1:n.1980G>A (POMGNT1)
ENST00000687613.1:n.2168G>A (POMGNT1)
ENST00000687683.1:c.1418G>A (POMGNT1)	ENSP00000508522.1:p.Trp473Ter
ENST00000688032.1:n.1980G>A (POMGNT1)
ENST00000688596.1:n.2069G>A (POMGNT1)
ENST00000688608.1:c.1319G>A (POMGNT1)	ENSP00000508890.1:p.Trp440Ter
ENST00000688919.1:n.2614G>A (POMGNT1)
ENST00000689031.1:n.1980G>A (POMGNT1)
ENST00000689717.1:n.1590G>A (POMGNT1)
ENST00000689756.1:c.*1050G>A (POMGNT1)	ENSP00000509023.1:n.*1050G>A
ENST00000690377.1:n.1765G>A (POMGNT1)
ENST00000690678.1:c.1418G>A (POMGNT1)	ENSP00000508703.1:p.Trp473Ter
ENST00000691209.1:c.*358G>A (POMGNT1)	ENSP00000510112.1:n.*358G>A
ENST00000691243.1:c.1418G>A (POMGNT1)	ENSP00000510654.1:p.Trp473Ter
ENST00000692169.1:n.1567G>A (POMGNT1)
ENST00000692202.1:n.1993G>A (POMGNT1)
ENST00000692322.1:c.*1270G>A (POMGNT1)	ENSP00000509017.1:n.*1270G>A
ENST00000692369.1:c.1418G>A (POMGNT1)	ENSP00000508453.1:p.Trp473Ter
ENST00000692599.1:n.1980G>A (POMGNT1)
ENST00000692635.1:c.*358G>A (POMGNT1)	ENSP00000508425.1:n.*358G>A
ENST00000693168.1:n.1679G>A (POMGNT1)
ENST00000693218.1:c.1418G>A (POMGNT1)	ENSP00000510577.1:p.Trp473Ter
ENST00000693223.1:n.2366G>A (POMGNT1)
ENST00000693365.1:n.4052G>A (POMGNT1)
ENST00000371984.8:c.1418G>A (POMGNT1) MANE Select	ENSP00000361052.3:p.Trp473Ter
ENST00000371984.7:c.1418G>A (POMGNT1)	ENSP00000361052.3:p.Trp473Ter
ENST00000371992.1:c.1418G>A (POMGNT1)	ENSP00000361060.1:p.Trp473Ter
ENST00000396420.7:c.*1087G>A (POMGNT1)	ENSP00000379698.3:n.*1087G>A
ENST00000463030.1:n.39G>A (POMGNT1)
ENST00000485714.1:n.804G>A (POMGNT1)
NM_001243766.1:c.1418G>A (POMGNT1)	NP_001230695.1:p.Trp473Ter
NM_001290129.1:c.1352G>A (POMGNT1)	NP_001277058.1:p.Trp451Ter
NM_001290130.1:c.989G>A (POMGNT1)	NP_001277059.1:p.Trp330Ter
NM_017739.3:c.1418G>A (POMGNT1)	NP_060209.3:p.Trp473Ter
XM_005271010.1:c.1418G>A (POMGNT1)	XP_005271067.1:p.Trp473Ter
XM_006710755.1:c.1418G>A (POMGNT1)	XP_006710818.1:p.Trp473Ter
XM_006710756.1:c.1418G>A (POMGNT1)	XP_006710819.1:p.Trp473Ter
XM_011540460.1:c.679-3983C>T (TSPAN1)	XP_011538762.1:n.679-3983C>T
XM_011540461.1:c.634-3983C>T (TSPAN1)	XP_011538763.1:n.634-3983C>T
XM_011541759.1:c.1352G>A (POMGNT1)	XP_011540061.1:p.Trp451Ter
XM_011541760.1:c.1352G>A (POMGNT1)	XP_011540062.1:p.Trp451Ter
XM_011541761.1:c.326G>A (POMGNT1)	XP_011540063.1:p.Trp109Ter
XR_946706.1:n.1578G>A (POMGNT1)
XM_011540460.3:c.679-3983C>T (TSPAN1)	XP_011538762.1:n.679-3983C>T
XM_011541760.3:c.1352G>A (POMGNT1)	XP_011540062.1:p.Trp451Ter
XM_017001690.1:c.1418G>A (POMGNT1)	XP_016857179.1:p.Trp473Ter
NM_001243766.2:c.1418G>A (POMGNT1)	NP_001230695.2:p.Trp473Ter
NM_001290129.2:c.1352G>A (POMGNT1)	NP_001277058.2:p.Trp451Ter
NM_001290130.2:c.989G>A (POMGNT1)	NP_001277059.2:p.Trp330Ter
NM_017739.4:c.1418G>A (POMGNT1) MANE Select	NP_060209.4:p.Trp473Ter