Canonical Allele Identifier: CA2695198023

Gene: POMGNT1 TSPAN1

Linked Data

• ClinVar Variation Id: 2677980
• ClinVar RCV Id: RCV003471727

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46192206del , CM000663.2:g.46192206del	GRCh38
NC_000001.10:g.46657878del , CM000663.1:g.46657878del	GRCh37
NC_000001.9:g.46430465del	NCBI36
NG_009205.2:g.33100del
NG_009205.3:g.33100del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396420.8:c.1431del (POMGNT1)	ENSP00000379698.4:p.Met477IlefsTer?
ENST00000477114.2:n.1993del (POMGNT1)
ENST00000497439.6:n.1603del (POMGNT1)
ENST00000684817.1:n.1791del (POMGNT1)
ENST00000684898.1:n.1993del (POMGNT1)
ENST00000685230.1:c.*741del (POMGNT1)	ENSP00000510305.1:n.*741del
ENST00000685275.1:n.1978del (POMGNT1)
ENST00000685444.1:c.1332del (POMGNT1)	ENSP00000510762.1:p.Met444IlefsTer?
ENST00000685704.1:n.1993del (POMGNT1)
ENST00000685775.1:n.2958del (POMGNT1)
ENST00000685833.1:n.2309del (POMGNT1)
ENST00000686252.1:n.2505del (POMGNT1)
ENST00000686379.1:c.*555del (POMGNT1)	ENSP00000508913.1:n.*555del
ENST00000686724.1:n.1603del (POMGNT1)
ENST00000686737.1:c.1431del (POMGNT1)	ENSP00000508736.1:p.Met477IlefsTer?
ENST00000687112.1:n.2297del (POMGNT1)
ENST00000687149.1:c.1431del (POMGNT1)	ENSP00000509745.1:p.Met477IlefsTer?
ENST00000687197.1:c.*371del (POMGNT1)	ENSP00000510749.1:n.*371del
ENST00000687235.1:n.1993del (POMGNT1)
ENST00000687613.1:n.2181del (POMGNT1)
ENST00000687683.1:c.1431del (POMGNT1)	ENSP00000508522.1:p.Met477IlefsTer?
ENST00000688032.1:n.1993del (POMGNT1)
ENST00000688596.1:n.2082del (POMGNT1)
ENST00000688608.1:c.1332del (POMGNT1)	ENSP00000508890.1:p.Met444IlefsTer?
ENST00000688919.1:n.2627del (POMGNT1)
ENST00000689031.1:n.1993del (POMGNT1)
ENST00000689717.1:n.1603del (POMGNT1)
ENST00000689756.1:c.*1063del (POMGNT1)	ENSP00000509023.1:n.*1063del
ENST00000690377.1:n.1778del (POMGNT1)
ENST00000690678.1:c.1431del (POMGNT1)	ENSP00000508703.1:p.Met477IlefsTer?
ENST00000691209.1:c.*371del (POMGNT1)	ENSP00000510112.1:n.*371del
ENST00000691243.1:c.1431del (POMGNT1)	ENSP00000510654.1:p.Met477IlefsTer?
ENST00000692169.1:n.1580del (POMGNT1)
ENST00000692202.1:n.2006del (POMGNT1)
ENST00000692322.1:c.*1283del (POMGNT1)	ENSP00000509017.1:n.*1283del
ENST00000692369.1:c.1431del (POMGNT1)	ENSP00000508453.1:p.Met477IlefsTer?
ENST00000692599.1:n.1993del (POMGNT1)
ENST00000692635.1:c.*371del (POMGNT1)	ENSP00000508425.1:n.*371del
ENST00000693168.1:n.1692del (POMGNT1)
ENST00000693218.1:c.1431del (POMGNT1)	ENSP00000510577.1:p.Met477IlefsTer?
ENST00000693223.1:n.2379del (POMGNT1)
ENST00000693365.1:n.4065del (POMGNT1)
ENST00000371984.8:c.1431del (POMGNT1) MANE Select	ENSP00000361052.3:p.Met477IlefsTer?
ENST00000371984.7:c.1431del (POMGNT1)	ENSP00000361052.3:p.Met477IlefsTer?
ENST00000371992.1:c.1431del (POMGNT1)	ENSP00000361060.1:p.Met477IlefsTer?
ENST00000396420.7:c.*1100del (POMGNT1)	ENSP00000379698.3:n.*1100del
ENST00000463030.1:n.52del (POMGNT1)
ENST00000485714.1:n.817del (POMGNT1)
NM_001243766.1:c.1431del (POMGNT1)	NP_001230695.1:p.Met477IlefsTer?
NM_001290129.1:c.1365del (POMGNT1)	NP_001277058.1:p.Met455IlefsTer?
NM_001290130.1:c.1002del (POMGNT1)	NP_001277059.1:p.Met334IlefsTer?
NM_017739.3:c.1431del (POMGNT1)	NP_060209.3:p.Met477IlefsTer?
XM_005271010.1:c.1431del (POMGNT1)	XP_005271067.1:p.Met477IlefsTer?
XM_006710755.1:c.1431del (POMGNT1)	XP_006710818.1:p.Met477IlefsTer?
XM_006710756.1:c.1431del (POMGNT1)	XP_006710819.1:p.Met477IlefsTer?
XM_011540460.1:c.679-3996del (TSPAN1)	XP_011538762.1:n.679-3996del
XM_011540461.1:c.634-3996del (TSPAN1)	XP_011538763.1:n.634-3996del
XM_011541759.1:c.1365del (POMGNT1)	XP_011540061.1:p.Met455IlefsTer?
XM_011541760.1:c.1365del (POMGNT1)	XP_011540062.1:p.Met455IlefsTer?
XM_011541761.1:c.339del (POMGNT1)	XP_011540063.1:p.Met113IlefsTer?
XR_946706.1:n.1591del (POMGNT1)
XM_011540460.3:c.679-3996del (TSPAN1)	XP_011538762.1:n.679-3996del
XM_011541760.3:c.1365del (POMGNT1)	XP_011540062.1:p.Met455IlefsTer?
XM_017001690.1:c.1431del (POMGNT1)	XP_016857179.1:p.Met477IlefsTer?
NM_001243766.2:c.1431del (POMGNT1)	NP_001230695.2:p.Met477IlefsTer?
NM_001290129.2:c.1365del (POMGNT1)	NP_001277058.2:p.Met455IlefsTer?
NM_001290130.2:c.1002del (POMGNT1)	NP_001277059.2:p.Met334IlefsTer?
NM_017739.4:c.1431del (POMGNT1) MANE Select	NP_060209.4:p.Met477IlefsTer?