Canonical Allele Identifier: CA1950968492

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8102054_8102055delinsCA , CM000673.2:g.8102054_8102055delinsCA GRCh38
NC_000011.9:g.8123601_8123602delinsCA , CM000673.1:g.8123601_8123602delinsCA GRCh37
NC_000011.8:g.8080177_8080178delinsCA NCBI36
NG_029912.1:g.68422_68423delinsCA
NG_030416.2:g.71989_71990delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*435_*436delinsCA (TUB) MANE Select ENSP00000299506.3:n.*435_*436delinsCA
ENST00000305253.8:c.*435_*436delinsCA (TUB) ENSP00000305426.4:n.*435_*436delinsCA
NM_003320.4:c.*435_*436delinsCA (TUB) NP_003311.2:n.*435_*436delinsCA
NM_177972.2:c.*435_*436delinsCA (TUB) NP_813977.1:n.*435_*436delinsCA
XM_005253109.2:c.*435_*436delinsCA (TUB) XP_005253166.1:n.*435_*436delinsCA
XM_011520344.1:c.*435_*436delinsCA (TUB) XP_011518646.1:n.*435_*436delinsCA
XR_428851.2:n.1484-7896_1484-7895delinsTG (RIC3)
XR_930896.1:n.1546+5280_1546+5281delinsTG (RIC3)
XR_930900.1:n.1547-4333_1547-4332delinsTG (RIC3)
NR_144485.1:n.1519+5280_1519+5281delinsTG (RIC3)
XM_005253109.3:c.*435_*436delinsCA (TUB) XP_005253166.1:n.*435_*436delinsCA
XM_011520344.2:c.*435_*436delinsCA (TUB) XP_011518646.1:n.*435_*436delinsCA
XR_001747957.2:n.1335-7896_1335-7895delinsTG (RIC3)
XR_428851.4:n.1422-7896_1422-7895delinsTG (RIC3)
XR_930896.3:n.1484+5280_1484+5281delinsTG (RIC3)
XR_930900.3:n.1485-4333_1485-4332delinsTG (RIC3)
NM_177972.3:c.*435_*436delinsCA (TUB) MANE Select NP_813977.1:n.*435_*436delinsCA
NR_144485.2:n.1450+5280_1450+5281delinsTG (RIC3)
NM_003320.5:c.*435_*436delinsCA (TUB) NP_003311.2:n.*435_*436delinsCA