Canonical Allele Identifier: CA1180934265

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837751C= , CM000663.2:g.92837751C= GRCh38
NC_000001.10:g.93303308C= , CM000663.1:g.93303308C= GRCh37
NC_000001.9:g.93075896C= NCBI36
NG_011779.1:g.10715C=
NG_033051.1:g.128772G=
NG_011779.2:g.10766C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+118C= (RPL5) MANE Select ENSP00000359345.2:n.705+118C=
ENST00000645119.1:c.325-2800C= (RPL5) ENSP00000493811.1:n.325-2800C=
ENST00000645300.1:c.555+118C= (RPL5) ENSP00000495589.1:n.555+118C=
ENST00000645908.1:n.557C= (RPL5)
ENST00000370321.7:c.705+118C= (RPL5) ENSP00000359345.2:n.705+118C=
ENST00000497519.1:n.1024+118C= (RPL5)
ENST00000615519.4:c.475-4717G= (DIPK1A) ENSP00000483279.1:n.475-4717G=
NM_000969.3:c.705+118C= (RPL5) NP_000960.2:n.705+118C=
NM_001252273.1:c.475-4717G= (DIPK1A) NP_001239202.1:n.475-4717G=
NM_000969.5:c.705+118C= (RPL5) MANE Select NP_000960.2:n.705+118C=
NR_146333.1:n.764+118C= (RPL5)
NM_001252273.2:c.475-4717G= (DIPK1A) NP_001239202.1:n.475-4717G=