Canonical Allele Identifier: CA2790353760

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101858_8101859insGACCC , CM000673.2:g.8101858_8101859insGACCC GRCh38
NC_000011.9:g.8123405_8123406insGACCC , CM000673.1:g.8123405_8123406insGACCC GRCh37
NC_000011.8:g.8079981_8079982insGACCC NCBI36
NG_029912.1:g.68226_68227insGACCC
NG_030416.2:g.72187_72188insGTCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*239_*240insGACCC (TUB) MANE Select ENSP00000299506.3:n.*239_*240insGACCC
ENST00000299506.2:c.*239_*240insGACCC (TUB) ENSP00000299506.2:n.*239_*240insGACCC
ENST00000305253.8:c.*239_*240insGACCC (TUB) ENSP00000305426.4:n.*239_*240insGACCC
NM_003320.4:c.*239_*240insGACCC (TUB) NP_003311.2:n.*239_*240insGACCC
NM_177972.2:c.*239_*240insGACCC (TUB) NP_813977.1:n.*239_*240insGACCC
XM_005253109.2:c.*239_*240insGACCC (TUB) XP_005253166.1:n.*239_*240insGACCC
XM_011520344.1:c.*239_*240insGACCC (TUB) XP_011518646.1:n.*239_*240insGACCC
XR_428851.2:n.1484-7698_1484-7697insGTCGG (RIC3)
XR_930896.1:n.1546+5478_1546+5479insGTCGG (RIC3)
XR_930900.1:n.1547-4135_1547-4134insGTCGG (RIC3)
NR_144485.1:n.1519+5478_1519+5479insGTCGG (RIC3)
XM_005253109.3:c.*239_*240insGACCC (TUB) XP_005253166.1:n.*239_*240insGACCC
XM_011520344.2:c.*239_*240insGACCC (TUB) XP_011518646.1:n.*239_*240insGACCC
XR_001747957.2:n.1335-7698_1335-7697insGTCGG (RIC3)
XR_428851.4:n.1422-7698_1422-7697insGTCGG (RIC3)
XR_930896.3:n.1484+5478_1484+5479insGTCGG (RIC3)
XR_930900.3:n.1485-4135_1485-4134insGTCGG (RIC3)
NM_177972.3:c.*239_*240insGACCC (TUB) MANE Select NP_813977.1:n.*239_*240insGACCC
NR_144485.2:n.1450+5478_1450+5479insGTCGG (RIC3)
NM_003320.5:c.*239_*240insGACCC (TUB) NP_003311.2:n.*239_*240insGACCC