Canonical Allele Identifier: CA379572734

Gene: TUB RIC3

Linked Data

• MyVariant Identifiers: chr11:g.8123155G>T (hg19) ; chr11:g.8101608G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8101608G>T , CM000673.2:g.8101608G>T	GRCh38
NC_000011.9:g.8123155G>T , CM000673.1:g.8123155G>T	GRCh37
NC_000011.8:g.8079731G>T	NCBI36
NG_029912.1:g.67976G>T
NG_030416.2:g.72436C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.1510G>T (TUB) MANE Select	ENSP00000299506.3:p.Ala504Ser
ENST00000299506.2:c.1510G>T (TUB)	ENSP00000299506.2:p.Ala504Ser
ENST00000305253.8:c.1675G>T (TUB)	ENSP00000305426.4:p.Ala559Ser
ENST00000534099.5:c.1528G>T (TUB)	ENSP00000434400.1:p.Ala510Ser
NM_003320.4:c.1675G>T (TUB)	NP_003311.2:p.Ala559Ser
NM_177972.2:c.1510G>T (TUB)	NP_813977.1:p.Ala504Ser
XM_005253109.2:c.1636G>T (TUB)	XP_005253166.1:p.Ala546Ser
XM_011520344.1:c.1546G>T (TUB)	XP_011518646.1:p.Ala516Ser
XR_428851.2:n.1484-7449C>A (RIC3)
XR_930896.1:n.1546+5727C>A (RIC3)
XR_930900.1:n.1547-3886C>A (RIC3)
NR_144485.1:n.1519+5727C>A (RIC3)
XM_005253109.3:c.1636G>T (TUB)	XP_005253166.1:p.Ala546Ser
XM_011520344.2:c.1546G>T (TUB)	XP_011518646.1:p.Ala516Ser
XR_001747957.2:n.1335-7449C>A (RIC3)
XR_428851.4:n.1422-7449C>A (RIC3)
XR_930896.3:n.1484+5727C>A (RIC3)
XR_930900.3:n.1485-3886C>A (RIC3)
NM_177972.3:c.1510G>T (TUB) MANE Select	NP_813977.1:p.Ala504Ser
NR_144485.2:n.1450+5727C>A (RIC3)
NM_003320.5:c.1675G>T (TUB)	NP_003311.2:p.Ala559Ser