Canonical Allele Identifier: CA1950970894

Gene: RIC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8128448_8128449delinsAG , CM000673.2:g.8128448_8128449delinsAG	GRCh38
NC_000011.9:g.8149995_8149996delinsAG , CM000673.1:g.8149995_8149996delinsAG	GRCh37
NC_000011.8:g.8106571_8106572delinsAG	NCBI36
NG_030416.1:g.45595_45596delinsCT
NG_030416.2:g.45595_45596delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699457.1:n.24_25delinsCT
ENST00000309737.11:c.522-1642_522-1641delinsCT MANE Select	ENSP00000308820.6:n.522-1642_522-1641delinsCT
ENST00000309737.10:c.522-1642_522-1641delinsCT	ENSP00000308820.6:n.522-1642_522-1641delinsCT
ENST00000335425.7:c.125-17312_125-17311delinsCT	ENSP00000333988.7:n.125-17312_125-17311delinsCT
ENST00000343202.8:c.522-1645_522-1644delinsCT	ENSP00000344904.4:n.522-1645_522-1644delinsCT
ENST00000425599.6:c.427+9823_427+9824delinsCT	ENSP00000395320.2:n.427+9823_427+9824delinsCT
ENST00000524799.5:n.383-1645_383-1644delinsCT
ENST00000526962.1:c.125-1645_125-1644delinsCT	ENSP00000434787.1:n.125-1645_125-1644delinsCT
ENST00000528463.5:c.*439-1642_*439-1641delinsCT	ENSP00000435244.1:n.*439-1642_*439-1641delinsCT
ENST00000530060.5:n.602-95_602-94delinsCT
ENST00000531450.1:c.522-1558_522-1557delinsCT	ENSP00000431658.1:n.522-1558_522-1557delinsCT
NM_001135109.2:c.125-17312_125-17311delinsCT	NP_001128581.1:n.125-17312_125-17311delinsCT
NM_001206671.2:c.522-1642_522-1641delinsCT	NP_001193600.1:n.522-1642_522-1641delinsCT
NM_001206672.2:c.427+9823_427+9824delinsCT	NP_001193601.1:n.427+9823_427+9824delinsCT
NM_024557.4:c.522-1645_522-1644delinsCT	NP_078833.3:n.522-1645_522-1644delinsCT
NR_045405.1:n.625-1642_625-1641delinsCT
XM_006718317.2:c.522-1558_522-1557delinsCT	XP_006718380.1:n.522-1558_522-1557delinsCT
XM_006718318.2:c.522-1645_522-1644delinsCT	XP_006718381.1:n.522-1645_522-1644delinsCT
XR_428848.2:n.616-1558_616-1557delinsCT
XR_428851.2:n.616-1558_616-1557delinsCT
XR_930896.1:n.616-1558_616-1557delinsCT
XR_930897.1:n.616-1558_616-1557delinsCT
XR_930898.1:n.616-1558_616-1557delinsCT
XR_930899.1:n.616-1558_616-1557delinsCT
XR_930900.1:n.616-1558_616-1557delinsCT
XR_930901.1:n.616-1642_616-1641delinsCT
XR_930902.1:n.616-1645_616-1644delinsCT
XR_930903.1:n.617-1642_617-1641delinsCT
XR_930904.1:n.602-158_602-157delinsCT
XR_930905.1:n.602-95_602-94delinsCT
XR_930906.1:n.616-95_616-94delinsCT
NM_001135109.3:c.125-17312_125-17311delinsCT	NP_001128581.1:n.125-17312_125-17311delinsCT
NM_001206671.3:c.522-1642_522-1641delinsCT	NP_001193600.1:n.522-1642_522-1641delinsCT
NM_001206672.3:c.427+9823_427+9824delinsCT	NP_001193601.1:n.427+9823_427+9824delinsCT
NM_001346690.1:c.-98-95_-98-94delinsCT	NP_001333619.1:n.-98-95_-98-94delinsCT
NM_001346691.1:c.521+8929_521+8930delinsCT	NP_001333620.1:n.521+8929_521+8930delinsCT
NM_001346692.1:c.375-1645_375-1644delinsCT	NP_001333621.1:n.375-1645_375-1644delinsCT
NM_001346693.1:c.375-1558_375-1557delinsCT	NP_001333622.1:n.375-1558_375-1557delinsCT
NM_001346694.1:c.375-1642_375-1641delinsCT	NP_001333623.1:n.375-1642_375-1641delinsCT
NM_024557.5:c.522-1645_522-1644delinsCT	NP_078833.3:n.522-1645_522-1644delinsCT
NR_144484.1:n.533-1645_533-1644delinsCT
NR_144485.1:n.676-1645_676-1644delinsCT
NR_144497.1:n.230-1645_230-1644delinsCT
XM_006718317.4:c.522-1558_522-1557delinsCT	XP_006718380.1:n.522-1558_522-1557delinsCT
XM_006718318.4:c.522-1645_522-1644delinsCT	XP_006718381.1:n.522-1645_522-1644delinsCT
XM_017018287.2:c.522-1558_522-1557delinsCT	XP_016873776.1:n.522-1558_522-1557delinsCT
XM_024448684.1:c.375-1645_375-1644delinsCT	XP_024304452.1:n.375-1645_375-1644delinsCT
XM_024448685.1:c.522-158_522-157delinsCT	XP_024304453.1:n.522-158_522-157delinsCT
XM_024448686.1:c.522-158_522-157delinsCT	XP_024304454.1:n.522-158_522-157delinsCT
XR_001747957.2:n.554-1645_554-1644delinsCT
XR_001747959.2:n.2222-158_2222-157delinsCT
XR_002957192.1:n.554-1645_554-1644delinsCT
XR_002957193.1:n.554-1645_554-1644delinsCT
XR_002957194.1:n.622-1558_622-1557delinsCT
XR_002957195.1:n.553+8929_553+8930delinsCT
XR_428848.4:n.554-1558_554-1557delinsCT
XR_428851.4:n.554-1558_554-1557delinsCT
XR_930896.3:n.554-1558_554-1557delinsCT
XR_930897.3:n.554-1558_554-1557delinsCT
XR_930898.3:n.554-1558_554-1557delinsCT
XR_930900.3:n.554-1558_554-1557delinsCT
XR_930901.3:n.554-1642_554-1641delinsCT
XR_930903.3:n.622-1642_622-1641delinsCT
XR_930904.3:n.2222-158_2222-157delinsCT
XR_930905.3:n.2222-95_2222-94delinsCT
NM_001206671.4:c.522-1642_522-1641delinsCT MANE Select	NP_001193600.1:n.522-1642_522-1641delinsCT
NM_001135109.4:c.125-17312_125-17311delinsCT	NP_001128581.1:n.125-17312_125-17311delinsCT
NM_001206672.4:c.427+9823_427+9824delinsCT	NP_001193601.1:n.427+9823_427+9824delinsCT
NM_001346690.2:c.-98-95_-98-94delinsCT	NP_001333619.1:n.-98-95_-98-94delinsCT
NM_001346691.2:c.521+8929_521+8930delinsCT	NP_001333620.1:n.521+8929_521+8930delinsCT
NM_001346692.2:c.375-1645_375-1644delinsCT	NP_001333621.1:n.375-1645_375-1644delinsCT
NM_001346693.2:c.375-1558_375-1557delinsCT	NP_001333622.1:n.375-1558_375-1557delinsCT
NM_001346694.2:c.375-1642_375-1641delinsCT	NP_001333623.1:n.375-1642_375-1641delinsCT
NM_024557.6:c.522-1645_522-1644delinsCT	NP_078833.3:n.522-1645_522-1644delinsCT
NR_144484.2:n.464-1645_464-1644delinsCT
NR_144485.2:n.607-1645_607-1644delinsCT
NR_144497.2:n.161-1645_161-1644delinsCT