Canonical Allele Identifier: CA934893032

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101847_8101853del , CM000673.2:g.8101847_8101853del GRCh38
NC_000011.9:g.8123394_8123400del , CM000673.1:g.8123394_8123400del GRCh37
NC_000011.8:g.8079970_8079976del NCBI36
NG_029912.1:g.68215_68221del
NG_030416.2:g.72191_72197del

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.*228_*234del (TUB) MANE Select ENSP00000299506.3:n.*228_*234del
ENST00000299506.2:c.*228_*234del (TUB) ENSP00000299506.2:n.*228_*234del
ENST00000305253.8:c.*228_*234del (TUB) ENSP00000305426.4:n.*228_*234del
NM_003320.4:c.*228_*234del (TUB) NP_003311.2:n.*228_*234del
NM_177972.2:c.*228_*234del (TUB) NP_813977.1:n.*228_*234del
XM_005253109.2:c.*228_*234del (TUB) XP_005253166.1:n.*228_*234del
XM_011520344.1:c.*228_*234del (TUB) XP_011518646.1:n.*228_*234del
XR_428851.2:n.1484-7694_1484-7688del (RIC3)
XR_930896.1:n.1546+5482_1546+5488del (RIC3)
XR_930900.1:n.1547-4131_1547-4125del (RIC3)
NR_144485.1:n.1519+5482_1519+5488del (RIC3)
XM_005253109.3:c.*228_*234del (TUB) XP_005253166.1:n.*228_*234del
XM_011520344.2:c.*228_*234del (TUB) XP_011518646.1:n.*228_*234del
XR_001747957.2:n.1335-7694_1335-7688del (RIC3)
XR_428851.4:n.1422-7694_1422-7688del (RIC3)
XR_930896.3:n.1484+5482_1484+5488del (RIC3)
XR_930900.3:n.1485-4131_1485-4125del (RIC3)
NM_177972.3:c.*228_*234del (TUB) MANE Select NP_813977.1:n.*228_*234del
NR_144485.2:n.1450+5482_1450+5488del (RIC3)
NM_003320.5:c.*228_*234del (TUB) NP_003311.2:n.*228_*234del