Canonical Allele Identifier: CA1180933627

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92836210G= , CM000663.2:g.92836210G= GRCh38
NC_000001.10:g.93301767G= , CM000663.1:g.93301767G= GRCh37
NC_000001.9:g.93074355G= NCBI36
NG_011779.1:g.9174G=
NG_033051.1:g.130313C=
NG_011779.2:g.9225G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.345G= (RPL5) MANE Select ENSP00000359345.2:p.Met115=
ENST00000645119.1:c.324+1297G= (RPL5) ENSP00000493811.1:n.324+1297G=
ENST00000645300.1:c.195G= (RPL5) ENSP00000495589.1:p.Met65=
ENST00000645908.1:n.79G= (RPL5)
ENST00000315741.5:c.195G= (RPL5) ENSP00000359338.2:p.Met65=
ENST00000370321.7:c.345G= (RPL5) ENSP00000359345.2:p.Met115=
ENST00000461952.1:n.1055G= (RPL5)
ENST00000470843.5:c.*307G= (RPL5) ENSP00000473675.1:n.*307G=
ENST00000615519.4:c.475-3176C= (DIPK1A) ENSP00000483279.1:n.475-3176C=
NM_000969.3:c.345G= (RPL5) NP_000960.2:p.Met115=
NM_001252273.1:c.475-3176C= (DIPK1A) NP_001239202.1:n.475-3176C=
NM_000969.5:c.345G= (RPL5) MANE Select NP_000960.2:p.Met115=
NR_146333.1:n.421-17G= (RPL5)
NM_001252273.2:c.475-3176C= (DIPK1A) NP_001239202.1:n.475-3176C=