Canonical Allele Identifier: CA2612334552

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101858_8101859insCA , CM000673.2:g.8101858_8101859insCA GRCh38
NC_000011.9:g.8123405_8123406insCA , CM000673.1:g.8123405_8123406insCA GRCh37
NC_000011.8:g.8079981_8079982insCA NCBI36
NG_029912.1:g.68226_68227insCA
NG_030416.2:g.72185_72186insTG

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.*239_*240insCA (TUB) MANE Select ENSP00000299506.3:n.*239_*240insCA
ENST00000299506.2:c.*239_*240insCA (TUB) ENSP00000299506.2:n.*239_*240insCA
ENST00000305253.8:c.*239_*240insCA (TUB) ENSP00000305426.4:n.*239_*240insCA
NM_003320.4:c.*239_*240insCA (TUB) NP_003311.2:n.*239_*240insCA
NM_177972.2:c.*239_*240insCA (TUB) NP_813977.1:n.*239_*240insCA
XM_005253109.2:c.*239_*240insCA (TUB) XP_005253166.1:n.*239_*240insCA
XM_011520344.1:c.*239_*240insCA (TUB) XP_011518646.1:n.*239_*240insCA
XR_428851.2:n.1484-7700_1484-7699insTG (RIC3)
XR_930896.1:n.1546+5476_1546+5477insTG (RIC3)
XR_930900.1:n.1547-4137_1547-4136insTG (RIC3)
NR_144485.1:n.1519+5476_1519+5477insTG (RIC3)
XM_005253109.3:c.*239_*240insCA (TUB) XP_005253166.1:n.*239_*240insCA
XM_011520344.2:c.*239_*240insCA (TUB) XP_011518646.1:n.*239_*240insCA
XR_001747957.2:n.1335-7700_1335-7699insTG (RIC3)
XR_428851.4:n.1422-7700_1422-7699insTG (RIC3)
XR_930896.3:n.1484+5476_1484+5477insTG (RIC3)
XR_930900.3:n.1485-4137_1485-4136insTG (RIC3)
NM_177972.3:c.*239_*240insCA (TUB) MANE Select NP_813977.1:n.*239_*240insCA
NR_144485.2:n.1450+5476_1450+5477insTG (RIC3)
NM_003320.5:c.*239_*240insCA (TUB) NP_003311.2:n.*239_*240insCA