Canonical Allele Identifier: CA2790354720
Gene: RIC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8128072_8128073insGAGCTAT , CM000673.2:g.8128072_8128073insGAGCTAT GRCh38
NC_000011.9:g.8149619_8149620insGAGCTAT , CM000673.1:g.8149619_8149620insGAGCTAT GRCh37
NC_000011.8:g.8106195_8106196insGAGCTAT NCBI36
NG_030416.1:g.45971_45972insATAGCTC
NG_030416.2:g.45971_45972insATAGCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000699457.1:n.400_401insATAGCTC
ENST00000309737.11:c.522-1266_522-1265insATAGCTC MANE Select ENSP00000308820.6:n.522-1266_522-1265insATAGCTC
ENST00000309737.10:c.522-1266_522-1265insATAGCTC ENSP00000308820.6:n.522-1266_522-1265insATAGCTC
ENST00000335425.7:c.125-16936_125-16935insATAGCTC ENSP00000333988.7:n.125-16936_125-16935insATAGCTC
ENST00000343202.8:c.522-1269_522-1268insATAGCTC ENSP00000344904.4:n.522-1269_522-1268insATAGCTC
ENST00000425599.6:c.427+10199_427+10200insATAGCTC ENSP00000395320.2:n.427+10199_427+10200insATAGCTC
ENST00000524799.5:n.383-1269_383-1268insATAGCTC
ENST00000526962.1:c.125-1269_125-1268insATAGCTC ENSP00000434787.1:n.125-1269_125-1268insATAGCTC
ENST00000528463.5:c.*439-1266_*439-1265insATAGCTC ENSP00000435244.1:n.*439-1266_*439-1265insATAGCTC
ENST00000530060.5:n.737+146_737+147insATAGCTC
ENST00000531450.1:c.522-1182_522-1181insATAGCTC ENSP00000431658.1:n.522-1182_522-1181insATAGCTC
NM_001135109.2:c.125-16936_125-16935insATAGCTC NP_001128581.1:n.125-16936_125-16935insATAGCTC
NM_001206671.2:c.522-1266_522-1265insATAGCTC NP_001193600.1:n.522-1266_522-1265insATAGCTC
NM_001206672.2:c.427+10199_427+10200insATAGCTC NP_001193601.1:n.427+10199_427+10200insATAGCTC
NM_024557.4:c.522-1269_522-1268insATAGCTC NP_078833.3:n.522-1269_522-1268insATAGCTC
NR_045405.1:n.625-1266_625-1265insATAGCTC
XM_006718317.2:c.522-1182_522-1181insATAGCTC XP_006718380.1:n.522-1182_522-1181insATAGCTC
XM_006718318.2:c.522-1269_522-1268insATAGCTC XP_006718381.1:n.522-1269_522-1268insATAGCTC
XR_428848.2:n.616-1182_616-1181insATAGCTC
XR_428851.2:n.616-1182_616-1181insATAGCTC
XR_930896.1:n.616-1182_616-1181insATAGCTC
XR_930897.1:n.616-1182_616-1181insATAGCTC
XR_930898.1:n.616-1182_616-1181insATAGCTC
XR_930899.1:n.616-1182_616-1181insATAGCTC
XR_930900.1:n.616-1182_616-1181insATAGCTC
XR_930901.1:n.616-1266_616-1265insATAGCTC
XR_930902.1:n.616-1269_616-1268insATAGCTC
XR_930903.1:n.617-1266_617-1265insATAGCTC
XR_930904.1:n.674+146_674+147insATAGCTC
XR_930905.1:n.737+146_737+147insATAGCTC
XR_930906.1:n.751+146_751+147insATAGCTC
NM_001135109.3:c.125-16936_125-16935insATAGCTC NP_001128581.1:n.125-16936_125-16935insATAGCTC
NM_001206671.3:c.522-1266_522-1265insATAGCTC NP_001193600.1:n.522-1266_522-1265insATAGCTC
NM_001206672.3:c.427+10199_427+10200insATAGCTC NP_001193601.1:n.427+10199_427+10200insATAGCTC
NM_001346690.1:c.38+146_38+147insATAGCTC NP_001333619.1:n.38+146_38+147insATAGCTC
NM_001346691.1:c.521+9305_521+9306insATAGCTC NP_001333620.1:n.521+9305_521+9306insATAGCTC
NM_001346692.1:c.375-1269_375-1268insATAGCTC NP_001333621.1:n.375-1269_375-1268insATAGCTC
NM_001346693.1:c.375-1182_375-1181insATAGCTC NP_001333622.1:n.375-1182_375-1181insATAGCTC
NM_001346694.1:c.375-1266_375-1265insATAGCTC NP_001333623.1:n.375-1266_375-1265insATAGCTC
NM_024557.5:c.522-1269_522-1268insATAGCTC NP_078833.3:n.522-1269_522-1268insATAGCTC
NR_144484.1:n.533-1269_533-1268insATAGCTC
NR_144485.1:n.676-1269_676-1268insATAGCTC
NR_144497.1:n.230-1269_230-1268insATAGCTC
XM_006718317.4:c.522-1182_522-1181insATAGCTC XP_006718380.1:n.522-1182_522-1181insATAGCTC
XM_006718318.4:c.522-1269_522-1268insATAGCTC XP_006718381.1:n.522-1269_522-1268insATAGCTC
XM_017018287.2:c.522-1182_522-1181insATAGCTC XP_016873776.1:n.522-1182_522-1181insATAGCTC
XM_024448684.1:c.375-1269_375-1268insATAGCTC XP_024304452.1:n.375-1269_375-1268insATAGCTC
XM_024448685.1:c.*39+146_*39+147insATAGCTC XP_024304453.1:n.*39+146_*39+147insATAGCTC
XM_024448686.1:c.*39+146_*39+147insATAGCTC XP_024304454.1:n.*39+146_*39+147insATAGCTC
XR_001747957.2:n.554-1269_554-1268insATAGCTC
XR_001747959.2:n.2294+146_2294+147insATAGCTC
XR_002957192.1:n.554-1269_554-1268insATAGCTC
XR_002957193.1:n.554-1269_554-1268insATAGCTC
XR_002957194.1:n.622-1182_622-1181insATAGCTC
XR_002957195.1:n.553+9305_553+9306insATAGCTC
XR_428848.4:n.554-1182_554-1181insATAGCTC
XR_428851.4:n.554-1182_554-1181insATAGCTC
XR_930896.3:n.554-1182_554-1181insATAGCTC
XR_930897.3:n.554-1182_554-1181insATAGCTC
XR_930898.3:n.554-1182_554-1181insATAGCTC
XR_930900.3:n.554-1182_554-1181insATAGCTC
XR_930901.3:n.554-1266_554-1265insATAGCTC
XR_930903.3:n.622-1266_622-1265insATAGCTC
XR_930904.3:n.2294+146_2294+147insATAGCTC
XR_930905.3:n.2357+146_2357+147insATAGCTC
NM_001206671.4:c.522-1266_522-1265insATAGCTC MANE Select NP_001193600.1:n.522-1266_522-1265insATAGCTC
NM_001135109.4:c.125-16936_125-16935insATAGCTC NP_001128581.1:n.125-16936_125-16935insATAGCTC
NM_001206672.4:c.427+10199_427+10200insATAGCTC NP_001193601.1:n.427+10199_427+10200insATAGCTC
NM_001346690.2:c.38+146_38+147insATAGCTC NP_001333619.1:n.38+146_38+147insATAGCTC
NM_001346691.2:c.521+9305_521+9306insATAGCTC NP_001333620.1:n.521+9305_521+9306insATAGCTC
NM_001346692.2:c.375-1269_375-1268insATAGCTC NP_001333621.1:n.375-1269_375-1268insATAGCTC
NM_001346693.2:c.375-1182_375-1181insATAGCTC NP_001333622.1:n.375-1182_375-1181insATAGCTC
NM_001346694.2:c.375-1266_375-1265insATAGCTC NP_001333623.1:n.375-1266_375-1265insATAGCTC
NM_024557.6:c.522-1269_522-1268insATAGCTC NP_078833.3:n.522-1269_522-1268insATAGCTC
NR_144484.2:n.464-1269_464-1268insATAGCTC
NR_144485.2:n.607-1269_607-1268insATAGCTC
NR_144497.2:n.161-1269_161-1268insATAGCTC