Canonical Allele Identifier: CA2474081274

Gene: POMGNT1 TSPAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46190165C= , CM000663.2:g.46190165C=	GRCh38
NC_000001.10:g.46655837C= , CM000663.1:g.46655837C=	GRCh37
NC_000001.9:g.46428424C=	NCBI36
NG_009205.2:g.35141G=
NG_009205.3:g.35141G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396420.8:c.1650-176G= (POMGNT1)	ENSP00000379698.4:n.1650-176G=
ENST00000497439.6:n.1822-176G= (POMGNT1)
ENST00000684817.1:n.2010-176G= (POMGNT1)
ENST00000684898.1:n.2212-176G= (POMGNT1)
ENST00000685230.1:c.*960-176G= (POMGNT1)	ENSP00000510305.1:n.*960-176G=
ENST00000685275.1:n.2197-176G= (POMGNT1)
ENST00000685444.1:c.1551-176G= (POMGNT1)	ENSP00000510762.1:n.1551-176G=
ENST00000685704.1:n.2316-176G= (POMGNT1)
ENST00000685775.1:n.4999G= (POMGNT1)
ENST00000685833.1:n.4043-176G= (POMGNT1)
ENST00000686252.1:n.2724-176G= (POMGNT1)
ENST00000686379.1:c.*774-176G= (POMGNT1)	ENSP00000508913.1:n.*774-176G=
ENST00000686724.1:n.3337-176G= (POMGNT1)
ENST00000686737.1:c.1650-176G= (POMGNT1)	ENSP00000508736.1:n.1650-176G=
ENST00000687112.1:n.2516-176G= (POMGNT1)
ENST00000687149.1:c.1689-176G= (POMGNT1)	ENSP00000509745.1:n.1689-176G=
ENST00000687197.1:c.*590-176G= (POMGNT1)	ENSP00000510749.1:n.*590-176G=
ENST00000687235.1:n.3727-176G= (POMGNT1)
ENST00000687613.1:n.2290-176G= (POMGNT1)
ENST00000687683.1:c.1650-176G= (POMGNT1)	ENSP00000508522.1:n.1650-176G=
ENST00000688032.1:n.2187-176G= (POMGNT1)
ENST00000688596.1:n.2301-176G= (POMGNT1)
ENST00000688608.1:c.1551-176G= (POMGNT1)	ENSP00000508890.1:n.1551-176G=
ENST00000688919.1:n.3355G= (POMGNT1)
ENST00000689031.1:n.2102-176G= (POMGNT1)
ENST00000689717.1:n.2331G= (POMGNT1)
ENST00000689756.1:c.*1282-176G= (POMGNT1)	ENSP00000509023.1:n.*1282-176G=
ENST00000690377.1:n.1997-176G= (POMGNT1)
ENST00000690678.1:c.1650-176G= (POMGNT1)	ENSP00000508703.1:n.1650-176G=
ENST00000691209.1:c.*590-176G= (POMGNT1)	ENSP00000510112.1:n.*590-176G=
ENST00000691243.1:c.*41-176G= (POMGNT1)	ENSP00000510654.1:n.*41-176G=
ENST00000692202.1:n.2225-176G= (POMGNT1)
ENST00000692322.1:c.*1437-176G= (POMGNT1)	ENSP00000509017.1:n.*1437-176G=
ENST00000692369.1:c.1650-176G= (POMGNT1)	ENSP00000508453.1:n.1650-176G=
ENST00000692599.1:n.3525-176G= (POMGNT1)
ENST00000692635.1:c.*525-176G= (POMGNT1)	ENSP00000508425.1:n.*525-176G=
ENST00000693168.1:n.3426-176G= (POMGNT1)
ENST00000693218.1:c.*211-176G= (POMGNT1)	ENSP00000510577.1:n.*211-176G=
ENST00000693223.1:n.2598-176G= (POMGNT1)
ENST00000371984.8:c.1650-176G= (POMGNT1) MANE Select	ENSP00000361052.3:n.1650-176G=
ENST00000371984.7:c.1650-176G= (POMGNT1)	ENSP00000361052.3:n.1650-176G=
ENST00000371992.1:c.1650-176G= (POMGNT1)	ENSP00000361060.1:n.1650-176G=
ENST00000396420.7:c.*1319-176G= (POMGNT1)	ENSP00000379698.3:n.*1319-176G=
ENST00000480972.1:n.299-176G= (POMGNT1)
ENST00000485714.1:n.2858G= (POMGNT1)
NM_001243766.1:c.1650-176G= (POMGNT1)	NP_001230695.1:n.1650-176G=
NM_001290129.1:c.1584-176G= (POMGNT1)	NP_001277058.1:n.1584-176G=
NM_001290130.1:c.1221-176G= (POMGNT1)	NP_001277059.1:n.1221-176G=
NM_017739.3:c.1650-176G= (POMGNT1)	NP_060209.3:n.1650-176G=
XM_005271010.1:c.1650-176G= (POMGNT1)	XP_005271067.1:n.1650-176G=
XM_006710755.1:c.1650-176G= (POMGNT1)	XP_006710818.1:n.1650-176G=
XM_006710756.1:c.1650-176G= (POMGNT1)	XP_006710819.1:n.1650-176G=
XM_011540460.1:c.678+4857C= (TSPAN1)	XP_011538762.1:n.678+4857C=
XM_011540461.1:c.633+4857C= (TSPAN1)	XP_011538763.1:n.633+4857C=
XM_011541759.1:c.1584-176G= (POMGNT1)	XP_011540061.1:n.1584-176G=
XM_011541760.1:c.1584-176G= (POMGNT1)	XP_011540062.1:n.1584-176G=
XM_011541761.1:c.558-176G= (POMGNT1)	XP_011540063.1:n.558-176G=
XM_011540460.3:c.678+4857C= (TSPAN1)	XP_011538762.1:n.678+4857C=
XM_011541760.3:c.1584-176G= (POMGNT1)	XP_011540062.1:n.1584-176G=
XM_017001690.1:c.1650-176G= (POMGNT1)	XP_016857179.1:n.1650-176G=
NM_001243766.2:c.1650-176G= (POMGNT1)	NP_001230695.2:n.1650-176G=
NM_001290129.2:c.1584-176G= (POMGNT1)	NP_001277058.2:n.1584-176G=
NM_001290130.2:c.1221-176G= (POMGNT1)	NP_001277059.2:n.1221-176G=
NM_017739.4:c.1650-176G= (POMGNT1) MANE Select	NP_060209.4:n.1650-176G=