Canonical Allele Identifier: CA1180934118

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837357T= , CM000663.2:g.92837357T= GRCh38
NC_000001.10:g.93302914T= , CM000663.1:g.93302914T= GRCh37
NC_000001.9:g.93075502T= NCBI36
NG_011779.1:g.10321T=
NG_033051.1:g.129166A=
NG_011779.2:g.10372T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.528-99T= (RPL5) MANE Select ENSP00000359345.2:n.528-99T=
ENST00000645119.1:c.324+2444T= (RPL5) ENSP00000493811.1:n.324+2444T=
ENST00000645300.1:c.378-99T= (RPL5) ENSP00000495589.1:n.378-99T=
ENST00000645908.1:n.262-99T= (RPL5)
ENST00000315741.5:c.378-99T= (RPL5) ENSP00000359338.2:n.378-99T=
ENST00000370321.7:c.528-99T= (RPL5) ENSP00000359345.2:n.528-99T=
ENST00000497519.1:n.748T= (RPL5)
ENST00000615519.4:c.475-4323A= (DIPK1A) ENSP00000483279.1:n.475-4323A=
NM_000969.3:c.528-99T= (RPL5) NP_000960.2:n.528-99T=
NM_001252273.1:c.475-4323A= (DIPK1A) NP_001239202.1:n.475-4323A=
NR_000006.8:n.69T= (SNORD21)
NM_000969.5:c.528-99T= (RPL5) MANE Select NP_000960.2:n.528-99T=
NR_146333.1:n.587-99T= (RPL5)
NM_001252273.2:c.475-4323A= (DIPK1A) NP_001239202.1:n.475-4323A=