Canonical Allele Identifier: CA1950968429

Linked Data

dbSNP Id: rs1944327616
gnomAD v4: 11-8101982-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101982G>A , CM000673.2:g.8101982G>A GRCh38
NC_000011.9:g.8123529G>A , CM000673.1:g.8123529G>A GRCh37
NC_000011.8:g.8080105G>A NCBI36
NG_029912.1:g.68350G>A
NG_030416.2:g.72062C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.*363G>A (TUB) MANE Select ENSP00000299506.3:n.*363G>A
ENST00000305253.8:c.*363G>A (TUB) ENSP00000305426.4:n.*363G>A
NM_003320.4:c.*363G>A (TUB) NP_003311.2:n.*363G>A
NM_177972.2:c.*363G>A (TUB) NP_813977.1:n.*363G>A
XM_005253109.2:c.*363G>A (TUB) XP_005253166.1:n.*363G>A
XM_011520344.1:c.*363G>A (TUB) XP_011518646.1:n.*363G>A
XR_428851.2:n.1484-7823C>T (RIC3)
XR_930896.1:n.1546+5353C>T (RIC3)
XR_930900.1:n.1547-4260C>T (RIC3)
NR_144485.1:n.1519+5353C>T (RIC3)
XM_005253109.3:c.*363G>A (TUB) XP_005253166.1:n.*363G>A
XM_011520344.2:c.*363G>A (TUB) XP_011518646.1:n.*363G>A
XR_001747957.2:n.1335-7823C>T (RIC3)
XR_428851.4:n.1422-7823C>T (RIC3)
XR_930896.3:n.1484+5353C>T (RIC3)
XR_930900.3:n.1485-4260C>T (RIC3)
NM_177972.3:c.*363G>A (TUB) MANE Select NP_813977.1:n.*363G>A
NR_144485.2:n.1450+5353C>T (RIC3)
NM_003320.5:c.*363G>A (TUB) NP_003311.2:n.*363G>A