Canonical Allele Identifier: CA680727361

Linked Data

dbSNP Id: rs1348606152
gnomAD v4: 11-8101849-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101849T>C , CM000673.2:g.8101849T>C GRCh38
NC_000011.9:g.8123396T>C , CM000673.1:g.8123396T>C GRCh37
NC_000011.8:g.8079972T>C NCBI36
NG_029912.1:g.68217T>C
NG_030416.2:g.72195A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.*230T>C (TUB) MANE Select ENSP00000299506.3:n.*230T>C
ENST00000299506.2:c.*230T>C (TUB) ENSP00000299506.2:n.*230T>C
ENST00000305253.8:c.*230T>C (TUB) ENSP00000305426.4:n.*230T>C
NM_003320.4:c.*230T>C (TUB) NP_003311.2:n.*230T>C
NM_177972.2:c.*230T>C (TUB) NP_813977.1:n.*230T>C
XM_005253109.2:c.*230T>C (TUB) XP_005253166.1:n.*230T>C
XM_011520344.1:c.*230T>C (TUB) XP_011518646.1:n.*230T>C
XR_428851.2:n.1484-7690A>G (RIC3)
XR_930896.1:n.1546+5486A>G (RIC3)
XR_930900.1:n.1547-4127A>G (RIC3)
NR_144485.1:n.1519+5486A>G (RIC3)
XM_005253109.3:c.*230T>C (TUB) XP_005253166.1:n.*230T>C
XM_011520344.2:c.*230T>C (TUB) XP_011518646.1:n.*230T>C
XR_001747957.2:n.1335-7690A>G (RIC3)
XR_428851.4:n.1422-7690A>G (RIC3)
XR_930896.3:n.1484+5486A>G (RIC3)
XR_930900.3:n.1485-4127A>G (RIC3)
NM_177972.3:c.*230T>C (TUB) MANE Select NP_813977.1:n.*230T>C
NR_144485.2:n.1450+5486A>G (RIC3)
NM_003320.5:c.*230T>C (TUB) NP_003311.2:n.*230T>C