Canonical Allele Identifier: CA2790354723

Gene: RIC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8128084del , CM000673.2:g.8128084del	GRCh38
NC_000011.9:g.8149631del , CM000673.1:g.8149631del	GRCh37
NC_000011.8:g.8106207del	NCBI36
NG_030416.1:g.45960del
NG_030416.2:g.45960del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699457.1:n.389del
ENST00000309737.11:c.522-1277del MANE Select	ENSP00000308820.6:n.522-1277del
ENST00000309737.10:c.522-1277del	ENSP00000308820.6:n.522-1277del
ENST00000335425.7:c.125-16947del	ENSP00000333988.7:n.125-16947del
ENST00000343202.8:c.522-1280del	ENSP00000344904.4:n.522-1280del
ENST00000425599.6:c.427+10188del	ENSP00000395320.2:n.427+10188del
ENST00000524799.5:n.383-1280del
ENST00000526962.1:c.125-1280del	ENSP00000434787.1:n.125-1280del
ENST00000528463.5:c.*439-1277del	ENSP00000435244.1:n.*439-1277del
ENST00000530060.5:n.737+135del
ENST00000531450.1:c.522-1193del	ENSP00000431658.1:n.522-1193del
NM_001135109.2:c.125-16947del	NP_001128581.1:n.125-16947del
NM_001206671.2:c.522-1277del	NP_001193600.1:n.522-1277del
NM_001206672.2:c.427+10188del	NP_001193601.1:n.427+10188del
NM_024557.4:c.522-1280del	NP_078833.3:n.522-1280del
NR_045405.1:n.625-1277del
XM_006718317.2:c.522-1193del	XP_006718380.1:n.522-1193del
XM_006718318.2:c.522-1280del	XP_006718381.1:n.522-1280del
XR_428848.2:n.616-1193del
XR_428851.2:n.616-1193del
XR_930896.1:n.616-1193del
XR_930897.1:n.616-1193del
XR_930898.1:n.616-1193del
XR_930899.1:n.616-1193del
XR_930900.1:n.616-1193del
XR_930901.1:n.616-1277del
XR_930902.1:n.616-1280del
XR_930903.1:n.617-1277del
XR_930904.1:n.674+135del
XR_930905.1:n.737+135del
XR_930906.1:n.751+135del
NM_001135109.3:c.125-16947del	NP_001128581.1:n.125-16947del
NM_001206671.3:c.522-1277del	NP_001193600.1:n.522-1277del
NM_001206672.3:c.427+10188del	NP_001193601.1:n.427+10188del
NM_001346690.1:c.38+135del	NP_001333619.1:n.38+135del
NM_001346691.1:c.521+9294del	NP_001333620.1:n.521+9294del
NM_001346692.1:c.375-1280del	NP_001333621.1:n.375-1280del
NM_001346693.1:c.375-1193del	NP_001333622.1:n.375-1193del
NM_001346694.1:c.375-1277del	NP_001333623.1:n.375-1277del
NM_024557.5:c.522-1280del	NP_078833.3:n.522-1280del
NR_144484.1:n.533-1280del
NR_144485.1:n.676-1280del
NR_144497.1:n.230-1280del
XM_006718317.4:c.522-1193del	XP_006718380.1:n.522-1193del
XM_006718318.4:c.522-1280del	XP_006718381.1:n.522-1280del
XM_017018287.2:c.522-1193del	XP_016873776.1:n.522-1193del
XM_024448684.1:c.375-1280del	XP_024304452.1:n.375-1280del
XM_024448685.1:c.*39+135del	XP_024304453.1:n.*39+135del
XM_024448686.1:c.*39+135del	XP_024304454.1:n.*39+135del
XR_001747957.2:n.554-1280del
XR_001747959.2:n.2294+135del
XR_002957192.1:n.554-1280del
XR_002957193.1:n.554-1280del
XR_002957194.1:n.622-1193del
XR_002957195.1:n.553+9294del
XR_428848.4:n.554-1193del
XR_428851.4:n.554-1193del
XR_930896.3:n.554-1193del
XR_930897.3:n.554-1193del
XR_930898.3:n.554-1193del
XR_930900.3:n.554-1193del
XR_930901.3:n.554-1277del
XR_930903.3:n.622-1277del
XR_930904.3:n.2294+135del
XR_930905.3:n.2357+135del
NM_001206671.4:c.522-1277del MANE Select	NP_001193600.1:n.522-1277del
NM_001135109.4:c.125-16947del	NP_001128581.1:n.125-16947del
NM_001206672.4:c.427+10188del	NP_001193601.1:n.427+10188del
NM_001346690.2:c.38+135del	NP_001333619.1:n.38+135del
NM_001346691.2:c.521+9294del	NP_001333620.1:n.521+9294del
NM_001346692.2:c.375-1280del	NP_001333621.1:n.375-1280del
NM_001346693.2:c.375-1193del	NP_001333622.1:n.375-1193del
NM_001346694.2:c.375-1277del	NP_001333623.1:n.375-1277del
NM_024557.6:c.522-1280del	NP_078833.3:n.522-1280del
NR_144484.2:n.464-1280del
NR_144485.2:n.607-1280del
NR_144497.2:n.161-1280del