Canonical Allele Identifier: CA2790353720

Gene: TUB RIC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8101768A>G , CM000673.2:g.8101768A>G	GRCh38
NC_000011.9:g.8123315A>G , CM000673.1:g.8123315A>G	GRCh37
NC_000011.8:g.8079891A>G	NCBI36
NG_029912.1:g.68136A>G
NG_030416.2:g.72276T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.*149A>G (TUB) MANE Select	ENSP00000299506.3:n.*149A>G
ENST00000299506.2:c.*149A>G (TUB)	ENSP00000299506.2:n.*149A>G
ENST00000305253.8:c.*149A>G (TUB)	ENSP00000305426.4:n.*149A>G
ENST00000534099.5:c.*149A>G (TUB)	ENSP00000434400.1:n.*149A>G
NM_003320.4:c.*149A>G (TUB)	NP_003311.2:n.*149A>G
NM_177972.2:c.*149A>G (TUB)	NP_813977.1:n.*149A>G
XM_005253109.2:c.*149A>G (TUB)	XP_005253166.1:n.*149A>G
XM_011520344.1:c.*149A>G (TUB)	XP_011518646.1:n.*149A>G
XR_428851.2:n.1484-7609T>C (RIC3)
XR_930896.1:n.1546+5567T>C (RIC3)
XR_930900.1:n.1547-4046T>C (RIC3)
NR_144485.1:n.1519+5567T>C (RIC3)
XM_005253109.3:c.*149A>G (TUB)	XP_005253166.1:n.*149A>G
XM_011520344.2:c.*149A>G (TUB)	XP_011518646.1:n.*149A>G
XR_001747957.2:n.1335-7609T>C (RIC3)
XR_428851.4:n.1422-7609T>C (RIC3)
XR_930896.3:n.1484+5567T>C (RIC3)
XR_930900.3:n.1485-4046T>C (RIC3)
NM_177972.3:c.*149A>G (TUB) MANE Select	NP_813977.1:n.*149A>G
NR_144485.2:n.1450+5567T>C (RIC3)
NM_003320.5:c.*149A>G (TUB)	NP_003311.2:n.*149A>G