Canonical Allele Identifier: CA2612334153

Linked Data

gnomAD v4: 11-8101828-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101828G>A , CM000673.2:g.8101828G>A GRCh38
NC_000011.9:g.8123375G>A , CM000673.1:g.8123375G>A GRCh37
NC_000011.8:g.8079951G>A NCBI36
NG_029912.1:g.68196G>A
NG_030416.2:g.72216C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*209G>A (TUB) MANE Select ENSP00000299506.3:n.*209G>A
ENST00000299506.2:c.*209G>A (TUB) ENSP00000299506.2:n.*209G>A
ENST00000305253.8:c.*209G>A (TUB) ENSP00000305426.4:n.*209G>A
NM_003320.4:c.*209G>A (TUB) NP_003311.2:n.*209G>A
NM_177972.2:c.*209G>A (TUB) NP_813977.1:n.*209G>A
XM_005253109.2:c.*209G>A (TUB) XP_005253166.1:n.*209G>A
XM_011520344.1:c.*209G>A (TUB) XP_011518646.1:n.*209G>A
XR_428851.2:n.1484-7669C>T (RIC3)
XR_930896.1:n.1546+5507C>T (RIC3)
XR_930900.1:n.1547-4106C>T (RIC3)
NR_144485.1:n.1519+5507C>T (RIC3)
XM_005253109.3:c.*209G>A (TUB) XP_005253166.1:n.*209G>A
XM_011520344.2:c.*209G>A (TUB) XP_011518646.1:n.*209G>A
XR_001747957.2:n.1335-7669C>T (RIC3)
XR_428851.4:n.1422-7669C>T (RIC3)
XR_930896.3:n.1484+5507C>T (RIC3)
XR_930900.3:n.1485-4106C>T (RIC3)
NM_177972.3:c.*209G>A (TUB) MANE Select NP_813977.1:n.*209G>A
NR_144485.2:n.1450+5507C>T (RIC3)
NM_003320.5:c.*209G>A (TUB) NP_003311.2:n.*209G>A