Canonical Allele Identifier: CA1180932413

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92833456G= , CM000663.2:g.92833456G= GRCh38
NC_000001.10:g.93299013G= , CM000663.1:g.93299013G= GRCh37
NC_000001.9:g.93071601G= NCBI36
NG_011779.1:g.6420G=
NG_033051.1:g.133067C=
NG_011779.2:g.6471G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370321.8:c.71G= (RPL5) MANE Select ENSP00000359345.2:p.Arg24=
ENST00000645119.1:c.71G= (RPL5) ENSP00000493811.1:p.Arg24=
ENST00000645300.1:c.-77-89G= (RPL5) ENSP00000495589.1:n.-77-89G=
ENST00000646852.1:n.100G= (RPL5)
ENST00000315741.5:c.-80G= (RPL5) ENSP00000359338.2:n.-80G=
ENST00000370321.7:c.71G= (RPL5) ENSP00000359345.2:p.Arg24=
ENST00000461952.1:n.695G= (RPL5)
ENST00000470843.5:c.71G= (RPL5) ENSP00000473675.1:p.Arg24=
ENST00000615519.4:c.475-422C= (DIPK1A) ENSP00000483279.1:n.475-422C=
NM_000969.3:c.71G= (RPL5) NP_000960.2:p.Arg24=
NM_001252273.1:c.475-422C= (DIPK1A) NP_001239202.1:n.475-422C=
NM_000969.5:c.71G= (RPL5) MANE Select NP_000960.2:p.Arg24=
NR_146333.1:n.200G= (RPL5)
NM_001252273.2:c.475-422C= (DIPK1A) NP_001239202.1:n.475-422C=