Canonical Allele Identifier: CA2612334729

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101929_8101930insCTG , CM000673.2:g.8101929_8101930insCTG GRCh38
NC_000011.9:g.8123476_8123477insCTG , CM000673.1:g.8123476_8123477insCTG GRCh37
NC_000011.8:g.8080052_8080053insCTG NCBI36
NG_029912.1:g.68297_68298insCTG
NG_030416.2:g.72114_72115insCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*310_*311insCTG (TUB) MANE Select ENSP00000299506.3:n.*310_*311insCTG
ENST00000299506.2:c.*310_*311insCTG (TUB) ENSP00000299506.2:n.*310_*311insCTG
ENST00000305253.8:c.*310_*311insCTG (TUB) ENSP00000305426.4:n.*310_*311insCTG
NM_003320.4:c.*310_*311insCTG (TUB) NP_003311.2:n.*310_*311insCTG
NM_177972.2:c.*310_*311insCTG (TUB) NP_813977.1:n.*310_*311insCTG
XM_005253109.2:c.*310_*311insCTG (TUB) XP_005253166.1:n.*310_*311insCTG
XM_011520344.1:c.*310_*311insCTG (TUB) XP_011518646.1:n.*310_*311insCTG
XR_428851.2:n.1484-7771_1484-7770insCAG (RIC3)
XR_930896.1:n.1546+5405_1546+5406insCAG (RIC3)
XR_930900.1:n.1547-4208_1547-4207insCAG (RIC3)
NR_144485.1:n.1519+5405_1519+5406insCAG (RIC3)
XM_005253109.3:c.*310_*311insCTG (TUB) XP_005253166.1:n.*310_*311insCTG
XM_011520344.2:c.*310_*311insCTG (TUB) XP_011518646.1:n.*310_*311insCTG
XR_001747957.2:n.1335-7771_1335-7770insCAG (RIC3)
XR_428851.4:n.1422-7771_1422-7770insCAG (RIC3)
XR_930896.3:n.1484+5405_1484+5406insCAG (RIC3)
XR_930900.3:n.1485-4208_1485-4207insCAG (RIC3)
NM_177972.3:c.*310_*311insCTG (TUB) MANE Select NP_813977.1:n.*310_*311insCTG
NR_144485.2:n.1450+5405_1450+5406insCAG (RIC3)
NM_003320.5:c.*310_*311insCTG (TUB) NP_003311.2:n.*310_*311insCTG