Canonical Allele Identifier: CA934893037

Linked Data

gnomAD v3: 11-8101848-C-G
gnomAD v4: 11-8101848-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101848C>G , CM000673.2:g.8101848C>G GRCh38
NC_000011.9:g.8123395C>G , CM000673.1:g.8123395C>G GRCh37
NC_000011.8:g.8079971C>G NCBI36
NG_029912.1:g.68216C>G
NG_030416.2:g.72196G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.*229C>G (TUB) MANE Select ENSP00000299506.3:n.*229C>G
ENST00000299506.2:c.*229C>G (TUB) ENSP00000299506.2:n.*229C>G
ENST00000305253.8:c.*229C>G (TUB) ENSP00000305426.4:n.*229C>G
NM_003320.4:c.*229C>G (TUB) NP_003311.2:n.*229C>G
NM_177972.2:c.*229C>G (TUB) NP_813977.1:n.*229C>G
XM_005253109.2:c.*229C>G (TUB) XP_005253166.1:n.*229C>G
XM_011520344.1:c.*229C>G (TUB) XP_011518646.1:n.*229C>G
XR_428851.2:n.1484-7689G>C (RIC3)
XR_930896.1:n.1546+5487G>C (RIC3)
XR_930900.1:n.1547-4126G>C (RIC3)
NR_144485.1:n.1519+5487G>C (RIC3)
XM_005253109.3:c.*229C>G (TUB) XP_005253166.1:n.*229C>G
XM_011520344.2:c.*229C>G (TUB) XP_011518646.1:n.*229C>G
XR_001747957.2:n.1335-7689G>C (RIC3)
XR_428851.4:n.1422-7689G>C (RIC3)
XR_930896.3:n.1484+5487G>C (RIC3)
XR_930900.3:n.1485-4126G>C (RIC3)
NM_177972.3:c.*229C>G (TUB) MANE Select NP_813977.1:n.*229C>G
NR_144485.2:n.1450+5487G>C (RIC3)
NM_003320.5:c.*229C>G (TUB) NP_003311.2:n.*229C>G