Canonical Allele Identifier: CA1180932411

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92833454A= , CM000663.2:g.92833454A= GRCh38
NC_000001.10:g.93299011A= , CM000663.1:g.93299011A= GRCh37
NC_000001.9:g.93071599A= NCBI36
NG_011779.1:g.6418A=
NG_033051.1:g.133069T=
NG_011779.2:g.6469A=

Transcript Alleles

HGVS Amino-acid change
ENST00000370321.8:c.69A= (RPL5) MANE Select ENSP00000359345.2:p.Arg23=
ENST00000645119.1:c.69A= (RPL5) ENSP00000493811.1:p.Arg23=
ENST00000645300.1:c.-77-91A= (RPL5) ENSP00000495589.1:n.-77-91A=
ENST00000646852.1:n.98A= (RPL5)
ENST00000315741.5:c.-82A= (RPL5) ENSP00000359338.2:n.-82A=
ENST00000370321.7:c.69A= (RPL5) ENSP00000359345.2:p.Arg23=
ENST00000461952.1:n.693A= (RPL5)
ENST00000470843.5:c.69A= (RPL5) ENSP00000473675.1:p.Arg23=
ENST00000615519.4:c.475-420T= (DIPK1A) ENSP00000483279.1:n.475-420T=
NM_000969.3:c.69A= (RPL5) NP_000960.2:p.Arg23=
NM_001252273.1:c.475-420T= (DIPK1A) NP_001239202.1:n.475-420T=
NM_000969.5:c.69A= (RPL5) MANE Select NP_000960.2:p.Arg23=
NR_146333.1:n.198A= (RPL5)
NM_001252273.2:c.475-420T= (DIPK1A) NP_001239202.1:n.475-420T=