Canonical Allele Identifier: CA1950968335

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101867A= , CM000673.2:g.8101867A= GRCh38
NC_000011.9:g.8123414A= , CM000673.1:g.8123414A= GRCh37
NC_000011.8:g.8079990A= NCBI36
NG_029912.1:g.68235A=
NG_030416.2:g.72177T=

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.*248A= (TUB) MANE Select ENSP00000299506.3:n.*248A=
ENST00000299506.2:c.*248A= (TUB) ENSP00000299506.2:n.*248A=
ENST00000305253.8:c.*248A= (TUB) ENSP00000305426.4:n.*248A=
NM_003320.4:c.*248A= (TUB) NP_003311.2:n.*248A=
NM_177972.2:c.*248A= (TUB) NP_813977.1:n.*248A=
XM_005253109.2:c.*248A= (TUB) XP_005253166.1:n.*248A=
XM_011520344.1:c.*248A= (TUB) XP_011518646.1:n.*248A=
XR_428851.2:n.1484-7708T= (RIC3)
XR_930896.1:n.1546+5468T= (RIC3)
XR_930900.1:n.1547-4145T= (RIC3)
NR_144485.1:n.1519+5468T= (RIC3)
XM_005253109.3:c.*248A= (TUB) XP_005253166.1:n.*248A=
XM_011520344.2:c.*248A= (TUB) XP_011518646.1:n.*248A=
XR_001747957.2:n.1335-7708T= (RIC3)
XR_428851.4:n.1422-7708T= (RIC3)
XR_930896.3:n.1484+5468T= (RIC3)
XR_930900.3:n.1485-4145T= (RIC3)
NM_177972.3:c.*248A= (TUB) MANE Select NP_813977.1:n.*248A=
NR_144485.2:n.1450+5468T= (RIC3)
NM_003320.5:c.*248A= (TUB) NP_003311.2:n.*248A=