Canonical Allele Identifier: CA1950970899

Gene: RIC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8128453_8128454delinsAC , CM000673.2:g.8128453_8128454delinsAC	GRCh38
NC_000011.9:g.8150000_8150001delinsAC , CM000673.1:g.8150000_8150001delinsAC	GRCh37
NC_000011.8:g.8106576_8106577delinsAC	NCBI36
NG_030416.1:g.45590_45591delinsGT
NG_030416.2:g.45590_45591delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699457.1:n.19_20delinsGT
ENST00000309737.11:c.522-1647_522-1646delinsGT MANE Select	ENSP00000308820.6:n.522-1647_522-1646delinsGT
ENST00000309737.10:c.522-1647_522-1646delinsGT	ENSP00000308820.6:n.522-1647_522-1646delinsGT
ENST00000335425.7:c.125-17317_125-17316delinsGT	ENSP00000333988.7:n.125-17317_125-17316delinsGT
ENST00000343202.8:c.522-1650_522-1649delinsGT	ENSP00000344904.4:n.522-1650_522-1649delinsGT
ENST00000425599.6:c.427+9818_427+9819delinsGT	ENSP00000395320.2:n.427+9818_427+9819delinsGT
ENST00000524799.5:n.383-1650_383-1649delinsGT
ENST00000526962.1:c.125-1650_125-1649delinsGT	ENSP00000434787.1:n.125-1650_125-1649delinsGT
ENST00000528463.5:c.*439-1647_*439-1646delinsGT	ENSP00000435244.1:n.*439-1647_*439-1646delinsGT
ENST00000530060.5:n.602-100_602-99delinsGT
ENST00000531450.1:c.522-1563_522-1562delinsGT	ENSP00000431658.1:n.522-1563_522-1562delinsGT
NM_001135109.2:c.125-17317_125-17316delinsGT	NP_001128581.1:n.125-17317_125-17316delinsGT
NM_001206671.2:c.522-1647_522-1646delinsGT	NP_001193600.1:n.522-1647_522-1646delinsGT
NM_001206672.2:c.427+9818_427+9819delinsGT	NP_001193601.1:n.427+9818_427+9819delinsGT
NM_024557.4:c.522-1650_522-1649delinsGT	NP_078833.3:n.522-1650_522-1649delinsGT
NR_045405.1:n.625-1647_625-1646delinsGT
XM_006718317.2:c.522-1563_522-1562delinsGT	XP_006718380.1:n.522-1563_522-1562delinsGT
XM_006718318.2:c.522-1650_522-1649delinsGT	XP_006718381.1:n.522-1650_522-1649delinsGT
XR_428848.2:n.616-1563_616-1562delinsGT
XR_428851.2:n.616-1563_616-1562delinsGT
XR_930896.1:n.616-1563_616-1562delinsGT
XR_930897.1:n.616-1563_616-1562delinsGT
XR_930898.1:n.616-1563_616-1562delinsGT
XR_930899.1:n.616-1563_616-1562delinsGT
XR_930900.1:n.616-1563_616-1562delinsGT
XR_930901.1:n.616-1647_616-1646delinsGT
XR_930902.1:n.616-1650_616-1649delinsGT
XR_930903.1:n.617-1647_617-1646delinsGT
XR_930904.1:n.602-163_602-162delinsGT
XR_930905.1:n.602-100_602-99delinsGT
XR_930906.1:n.616-100_616-99delinsGT
NM_001135109.3:c.125-17317_125-17316delinsGT	NP_001128581.1:n.125-17317_125-17316delinsGT
NM_001206671.3:c.522-1647_522-1646delinsGT	NP_001193600.1:n.522-1647_522-1646delinsGT
NM_001206672.3:c.427+9818_427+9819delinsGT	NP_001193601.1:n.427+9818_427+9819delinsGT
NM_001346690.1:c.-98-100_-98-99delinsGT	NP_001333619.1:n.-98-100_-98-99delinsGT
NM_001346691.1:c.521+8924_521+8925delinsGT	NP_001333620.1:n.521+8924_521+8925delinsGT
NM_001346692.1:c.375-1650_375-1649delinsGT	NP_001333621.1:n.375-1650_375-1649delinsGT
NM_001346693.1:c.375-1563_375-1562delinsGT	NP_001333622.1:n.375-1563_375-1562delinsGT
NM_001346694.1:c.375-1647_375-1646delinsGT	NP_001333623.1:n.375-1647_375-1646delinsGT
NM_024557.5:c.522-1650_522-1649delinsGT	NP_078833.3:n.522-1650_522-1649delinsGT
NR_144484.1:n.533-1650_533-1649delinsGT
NR_144485.1:n.676-1650_676-1649delinsGT
NR_144497.1:n.230-1650_230-1649delinsGT
XM_006718317.4:c.522-1563_522-1562delinsGT	XP_006718380.1:n.522-1563_522-1562delinsGT
XM_006718318.4:c.522-1650_522-1649delinsGT	XP_006718381.1:n.522-1650_522-1649delinsGT
XM_017018287.2:c.522-1563_522-1562delinsGT	XP_016873776.1:n.522-1563_522-1562delinsGT
XM_024448684.1:c.375-1650_375-1649delinsGT	XP_024304452.1:n.375-1650_375-1649delinsGT
XM_024448685.1:c.522-163_522-162delinsGT	XP_024304453.1:n.522-163_522-162delinsGT
XM_024448686.1:c.522-163_522-162delinsGT	XP_024304454.1:n.522-163_522-162delinsGT
XR_001747957.2:n.554-1650_554-1649delinsGT
XR_001747959.2:n.2222-163_2222-162delinsGT
XR_002957192.1:n.554-1650_554-1649delinsGT
XR_002957193.1:n.554-1650_554-1649delinsGT
XR_002957194.1:n.622-1563_622-1562delinsGT
XR_002957195.1:n.553+8924_553+8925delinsGT
XR_428848.4:n.554-1563_554-1562delinsGT
XR_428851.4:n.554-1563_554-1562delinsGT
XR_930896.3:n.554-1563_554-1562delinsGT
XR_930897.3:n.554-1563_554-1562delinsGT
XR_930898.3:n.554-1563_554-1562delinsGT
XR_930900.3:n.554-1563_554-1562delinsGT
XR_930901.3:n.554-1647_554-1646delinsGT
XR_930903.3:n.622-1647_622-1646delinsGT
XR_930904.3:n.2222-163_2222-162delinsGT
XR_930905.3:n.2222-100_2222-99delinsGT
NM_001206671.4:c.522-1647_522-1646delinsGT MANE Select	NP_001193600.1:n.522-1647_522-1646delinsGT
NM_001135109.4:c.125-17317_125-17316delinsGT	NP_001128581.1:n.125-17317_125-17316delinsGT
NM_001206672.4:c.427+9818_427+9819delinsGT	NP_001193601.1:n.427+9818_427+9819delinsGT
NM_001346690.2:c.-98-100_-98-99delinsGT	NP_001333619.1:n.-98-100_-98-99delinsGT
NM_001346691.2:c.521+8924_521+8925delinsGT	NP_001333620.1:n.521+8924_521+8925delinsGT
NM_001346692.2:c.375-1650_375-1649delinsGT	NP_001333621.1:n.375-1650_375-1649delinsGT
NM_001346693.2:c.375-1563_375-1562delinsGT	NP_001333622.1:n.375-1563_375-1562delinsGT
NM_001346694.2:c.375-1647_375-1646delinsGT	NP_001333623.1:n.375-1647_375-1646delinsGT
NM_024557.6:c.522-1650_522-1649delinsGT	NP_078833.3:n.522-1650_522-1649delinsGT
NR_144484.2:n.464-1650_464-1649delinsGT
NR_144485.2:n.607-1650_607-1649delinsGT
NR_144497.2:n.161-1650_161-1649delinsGT