Canonical Allele Identifier: CA1143541083

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837368C= , CM000663.2:g.92837368C= GRCh38
NC_000001.10:g.93302925C= , CM000663.1:g.93302925C= GRCh37
NC_000001.9:g.93075513C= NCBI36
NG_011779.1:g.10332C=
NG_033051.1:g.129155G=
NG_011779.2:g.10383C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.528-88C= (RPL5) MANE Select ENSP00000359345.2:n.528-88C=
ENST00000645119.1:c.324+2455C= (RPL5) ENSP00000493811.1:n.324+2455C=
ENST00000645300.1:c.378-88C= (RPL5) ENSP00000495589.1:n.378-88C=
ENST00000645908.1:n.262-88C= (RPL5)
ENST00000315741.5:c.378-88C= (RPL5) ENSP00000359338.2:n.378-88C=
ENST00000370321.7:c.528-88C= (RPL5) ENSP00000359345.2:n.528-88C=
ENST00000497519.1:n.759C= (RPL5)
ENST00000615519.4:c.475-4334G= (DIPK1A) ENSP00000483279.1:n.475-4334G=
NM_000969.3:c.528-88C= (RPL5) NP_000960.2:n.528-88C=
NM_001252273.1:c.475-4334G= (DIPK1A) NP_001239202.1:n.475-4334G=
NR_000006.8:n.80C= (SNORD21)
NM_000969.5:c.528-88C= (RPL5) MANE Select NP_000960.2:n.528-88C=
NR_146333.1:n.587-88C= (RPL5)
NM_001252273.2:c.475-4334G= (DIPK1A) NP_001239202.1:n.475-4334G=