Canonical Allele Identifier: CA1950967921

Gene: TUB RIC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8101593T= , CM000673.2:g.8101593T=	GRCh38
NC_000011.9:g.8123140T= , CM000673.1:g.8123140T=	GRCh37
NC_000011.8:g.8079716T=	NCBI36
NG_029912.1:g.67961T=
NG_030416.2:g.72451A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.1495T= (TUB) MANE Select	ENSP00000299506.3:p.Phe499=
ENST00000299506.2:c.1495T= (TUB)	ENSP00000299506.2:p.Phe499=
ENST00000305253.8:c.1660T= (TUB)	ENSP00000305426.4:p.Phe554=
ENST00000534099.5:c.1513T= (TUB)	ENSP00000434400.1:p.Phe505=
NM_003320.4:c.1660T= (TUB)	NP_003311.2:p.Phe554=
NM_177972.2:c.1495T= (TUB)	NP_813977.1:p.Phe499=
XM_005253109.2:c.1621T= (TUB)	XP_005253166.1:p.Phe541=
XM_011520344.1:c.1531T= (TUB)	XP_011518646.1:p.Phe511=
XR_428851.2:n.1484-7434A= (RIC3)
XR_930896.1:n.1546+5742A= (RIC3)
XR_930900.1:n.1547-3871A= (RIC3)
NR_144485.1:n.1519+5742A= (RIC3)
XM_005253109.3:c.1621T= (TUB)	XP_005253166.1:p.Phe541=
XM_011520344.2:c.1531T= (TUB)	XP_011518646.1:p.Phe511=
XR_001747957.2:n.1335-7434A= (RIC3)
XR_428851.4:n.1422-7434A= (RIC3)
XR_930896.3:n.1484+5742A= (RIC3)
XR_930900.3:n.1485-3871A= (RIC3)
NM_177972.3:c.1495T= (TUB) MANE Select	NP_813977.1:p.Phe499=
NR_144485.2:n.1450+5742A= (RIC3)
NM_003320.5:c.1660T= (TUB)	NP_003311.2:p.Phe554=