Canonical Allele Identifier: CA2612334824

Linked Data

gnomAD v4: 11-8101960-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101960G>T , CM000673.2:g.8101960G>T GRCh38
NC_000011.9:g.8123507G>T , CM000673.1:g.8123507G>T GRCh37
NC_000011.8:g.8080083G>T NCBI36
NG_029912.1:g.68328G>T
NG_030416.2:g.72084C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.*341G>T (TUB) MANE Select ENSP00000299506.3:n.*341G>T
ENST00000299506.2:c.*341G>T (TUB) ENSP00000299506.2:n.*341G>T
ENST00000305253.8:c.*341G>T (TUB) ENSP00000305426.4:n.*341G>T
NM_003320.4:c.*341G>T (TUB) NP_003311.2:n.*341G>T
NM_177972.2:c.*341G>T (TUB) NP_813977.1:n.*341G>T
XM_005253109.2:c.*341G>T (TUB) XP_005253166.1:n.*341G>T
XM_011520344.1:c.*341G>T (TUB) XP_011518646.1:n.*341G>T
XR_428851.2:n.1484-7801C>A (RIC3)
XR_930896.1:n.1546+5375C>A (RIC3)
XR_930900.1:n.1547-4238C>A (RIC3)
NR_144485.1:n.1519+5375C>A (RIC3)
XM_005253109.3:c.*341G>T (TUB) XP_005253166.1:n.*341G>T
XM_011520344.2:c.*341G>T (TUB) XP_011518646.1:n.*341G>T
XR_001747957.2:n.1335-7801C>A (RIC3)
XR_428851.4:n.1422-7801C>A (RIC3)
XR_930896.3:n.1484+5375C>A (RIC3)
XR_930900.3:n.1485-4238C>A (RIC3)
NM_177972.3:c.*341G>T (TUB) MANE Select NP_813977.1:n.*341G>T
NR_144485.2:n.1450+5375C>A (RIC3)
NM_003320.5:c.*341G>T (TUB) NP_003311.2:n.*341G>T