Canonical Allele Identifier: CA1950968309

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101847_8101848delinsTC , CM000673.2:g.8101847_8101848delinsTC GRCh38
NC_000011.9:g.8123394_8123395delinsTC , CM000673.1:g.8123394_8123395delinsTC GRCh37
NC_000011.8:g.8079970_8079971delinsTC NCBI36
NG_029912.1:g.68215_68216delinsTC
NG_030416.2:g.72196_72197delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.*228_*229delinsTC (TUB) MANE Select ENSP00000299506.3:n.*228_*229delinsTC
ENST00000299506.2:c.*228_*229delinsTC (TUB) ENSP00000299506.2:n.*228_*229delinsTC
ENST00000305253.8:c.*228_*229delinsTC (TUB) ENSP00000305426.4:n.*228_*229delinsTC
NM_003320.4:c.*228_*229delinsTC (TUB) NP_003311.2:n.*228_*229delinsTC
NM_177972.2:c.*228_*229delinsTC (TUB) NP_813977.1:n.*228_*229delinsTC
XM_005253109.2:c.*228_*229delinsTC (TUB) XP_005253166.1:n.*228_*229delinsTC
XM_011520344.1:c.*228_*229delinsTC (TUB) XP_011518646.1:n.*228_*229delinsTC
XR_428851.2:n.1484-7689_1484-7688delinsGA (RIC3)
XR_930896.1:n.1546+5487_1546+5488delinsGA (RIC3)
XR_930900.1:n.1547-4126_1547-4125delinsGA (RIC3)
NR_144485.1:n.1519+5487_1519+5488delinsGA (RIC3)
XM_005253109.3:c.*228_*229delinsTC (TUB) XP_005253166.1:n.*228_*229delinsTC
XM_011520344.2:c.*228_*229delinsTC (TUB) XP_011518646.1:n.*228_*229delinsTC
XR_001747957.2:n.1335-7689_1335-7688delinsGA (RIC3)
XR_428851.4:n.1422-7689_1422-7688delinsGA (RIC3)
XR_930896.3:n.1484+5487_1484+5488delinsGA (RIC3)
XR_930900.3:n.1485-4126_1485-4125delinsGA (RIC3)
NM_177972.3:c.*228_*229delinsTC (TUB) MANE Select NP_813977.1:n.*228_*229delinsTC
NR_144485.2:n.1450+5487_1450+5488delinsGA (RIC3)
NM_003320.5:c.*228_*229delinsTC (TUB) NP_003311.2:n.*228_*229delinsTC