Canonical Allele Identifier: CA2474081306

Gene: POMGNT1 TSPAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46190235_46190236delinsAG , CM000663.2:g.46190235_46190236delinsAG	GRCh38
NC_000001.10:g.46655907_46655908delinsAG , CM000663.1:g.46655907_46655908delinsAG	GRCh37
NC_000001.9:g.46428494_46428495delinsAG	NCBI36
NG_009205.2:g.35070_35071delinsCT
NG_009205.3:g.35070_35071delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396420.8:c.1649+237_1649+238delinsCT (POMGNT1)	ENSP00000379698.4:n.1649+237_1649+238delinsCT
ENST00000497439.6:n.1821+237_1821+238delinsCT (POMGNT1)
ENST00000684817.1:n.2009+237_2009+238delinsCT (POMGNT1)
ENST00000684898.1:n.2211+237_2211+238delinsCT (POMGNT1)
ENST00000685230.1:c.*959+237_*959+238delinsCT (POMGNT1)	ENSP00000510305.1:n.*959+237_*959+238delinsCT
ENST00000685275.1:n.2196+237_2196+238delinsCT (POMGNT1)
ENST00000685444.1:c.1550+237_1550+238delinsCT (POMGNT1)	ENSP00000510762.1:n.1550+237_1550+238delinsCT
ENST00000685704.1:n.2315+237_2315+238delinsCT (POMGNT1)
ENST00000685775.1:n.4928_4929delinsCT (POMGNT1)
ENST00000685833.1:n.4042+237_4042+238delinsCT (POMGNT1)
ENST00000686252.1:n.2723+237_2723+238delinsCT (POMGNT1)
ENST00000686379.1:c.*773+237_*773+238delinsCT (POMGNT1)	ENSP00000508913.1:n.*773+237_*773+238delinsCT
ENST00000686724.1:n.3336+237_3336+238delinsCT (POMGNT1)
ENST00000686737.1:c.1649+237_1649+238delinsCT (POMGNT1)	ENSP00000508736.1:n.1649+237_1649+238delinsCT
ENST00000687112.1:n.2515+237_2515+238delinsCT (POMGNT1)
ENST00000687149.1:c.1688+237_1688+238delinsCT (POMGNT1)	ENSP00000509745.1:n.1688+237_1688+238delinsCT
ENST00000687197.1:c.*589+237_*589+238delinsCT (POMGNT1)	ENSP00000510749.1:n.*589+237_*589+238delinsCT
ENST00000687235.1:n.3726+237_3726+238delinsCT (POMGNT1)
ENST00000687613.1:n.2290-247_2290-246delinsCT (POMGNT1)
ENST00000687683.1:c.1649+237_1649+238delinsCT (POMGNT1)	ENSP00000508522.1:n.1649+237_1649+238delinsCT
ENST00000688032.1:n.2186+237_2186+238delinsCT (POMGNT1)
ENST00000688596.1:n.2300+237_2300+238delinsCT (POMGNT1)
ENST00000688608.1:c.1550+237_1550+238delinsCT (POMGNT1)	ENSP00000508890.1:n.1550+237_1550+238delinsCT
ENST00000688919.1:n.3284_3285delinsCT (POMGNT1)
ENST00000689031.1:n.2102-247_2102-246delinsCT (POMGNT1)
ENST00000689717.1:n.2260_2261delinsCT (POMGNT1)
ENST00000689756.1:c.*1281+237_*1281+238delinsCT (POMGNT1)	ENSP00000509023.1:n.*1281+237_*1281+238delinsCT
ENST00000690377.1:n.1996+237_1996+238delinsCT (POMGNT1)
ENST00000690678.1:c.1649+237_1649+238delinsCT (POMGNT1)	ENSP00000508703.1:n.1649+237_1649+238delinsCT
ENST00000691209.1:c.*589+237_*589+238delinsCT (POMGNT1)	ENSP00000510112.1:n.*589+237_*589+238delinsCT
ENST00000691243.1:c.*40+237_*40+238delinsCT (POMGNT1)	ENSP00000510654.1:n.*40+237_*40+238delinsCT
ENST00000692169.1:n.3550_3551delinsCT (POMGNT1)
ENST00000692202.1:n.2224+237_2224+238delinsCT (POMGNT1)
ENST00000692322.1:c.*1436+237_*1436+238delinsCT (POMGNT1)	ENSP00000509017.1:n.*1436+237_*1436+238delinsCT
ENST00000692369.1:c.1649+237_1649+238delinsCT (POMGNT1)	ENSP00000508453.1:n.1649+237_1649+238delinsCT
ENST00000692599.1:n.3524+237_3524+238delinsCT (POMGNT1)
ENST00000692635.1:c.*524+237_*524+238delinsCT (POMGNT1)	ENSP00000508425.1:n.*524+237_*524+238delinsCT
ENST00000693168.1:n.3425+237_3425+238delinsCT (POMGNT1)
ENST00000693218.1:c.*210+237_*210+238delinsCT (POMGNT1)	ENSP00000510577.1:n.*210+237_*210+238delinsCT
ENST00000693223.1:n.2597+237_2597+238delinsCT (POMGNT1)
ENST00000371984.8:c.1649+237_1649+238delinsCT (POMGNT1) MANE Select	ENSP00000361052.3:n.1649+237_1649+238delinsCT
ENST00000371984.7:c.1649+237_1649+238delinsCT (POMGNT1)	ENSP00000361052.3:n.1649+237_1649+238delinsCT
ENST00000371992.1:c.1649+237_1649+238delinsCT (POMGNT1)	ENSP00000361060.1:n.1649+237_1649+238delinsCT
ENST00000396420.7:c.*1318+237_*1318+238delinsCT (POMGNT1)	ENSP00000379698.3:n.*1318+237_*1318+238delinsCT
ENST00000480972.1:n.298+237_298+238delinsCT (POMGNT1)
ENST00000485714.1:n.2787_2788delinsCT (POMGNT1)
NM_001243766.1:c.1649+237_1649+238delinsCT (POMGNT1)	NP_001230695.1:n.1649+237_1649+238delinsCT
NM_001290129.1:c.1583+237_1583+238delinsCT (POMGNT1)	NP_001277058.1:n.1583+237_1583+238delinsCT
NM_001290130.1:c.1220+237_1220+238delinsCT (POMGNT1)	NP_001277059.1:n.1220+237_1220+238delinsCT
NM_017739.3:c.1649+237_1649+238delinsCT (POMGNT1)	NP_060209.3:n.1649+237_1649+238delinsCT
XM_005271010.1:c.1649+237_1649+238delinsCT (POMGNT1)	XP_005271067.1:n.1649+237_1649+238delinsCT
XM_006710755.1:c.1649+237_1649+238delinsCT (POMGNT1)	XP_006710818.1:n.1649+237_1649+238delinsCT
XM_006710756.1:c.1649+237_1649+238delinsCT (POMGNT1)	XP_006710819.1:n.1649+237_1649+238delinsCT
XM_011540460.1:c.678+4927_678+4928delinsAG (TSPAN1)	XP_011538762.1:n.678+4927_678+4928delinsAG
XM_011540461.1:c.633+4927_633+4928delinsAG (TSPAN1)	XP_011538763.1:n.633+4927_633+4928delinsAG
XM_011541759.1:c.1583+237_1583+238delinsCT (POMGNT1)	XP_011540061.1:n.1583+237_1583+238delinsCT
XM_011541760.1:c.1583+237_1583+238delinsCT (POMGNT1)	XP_011540062.1:n.1583+237_1583+238delinsCT
XM_011541761.1:c.557+237_557+238delinsCT (POMGNT1)	XP_011540063.1:n.557+237_557+238delinsCT
XM_011540460.3:c.678+4927_678+4928delinsAG (TSPAN1)	XP_011538762.1:n.678+4927_678+4928delinsAG
XM_011541760.3:c.1583+237_1583+238delinsCT (POMGNT1)	XP_011540062.1:n.1583+237_1583+238delinsCT
XM_017001690.1:c.1649+237_1649+238delinsCT (POMGNT1)	XP_016857179.1:n.1649+237_1649+238delinsCT
NM_001243766.2:c.1649+237_1649+238delinsCT (POMGNT1)	NP_001230695.2:n.1649+237_1649+238delinsCT
NM_001290129.2:c.1583+237_1583+238delinsCT (POMGNT1)	NP_001277058.2:n.1583+237_1583+238delinsCT
NM_001290130.2:c.1220+237_1220+238delinsCT (POMGNT1)	NP_001277059.2:n.1220+237_1220+238delinsCT
NM_017739.4:c.1649+237_1649+238delinsCT (POMGNT1) MANE Select	NP_060209.4:n.1649+237_1649+238delinsCT