Canonical Allele Identifier: CA1180934169

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837522C= , CM000663.2:g.92837522C= GRCh38
NC_000001.10:g.93303079C= , CM000663.1:g.93303079C= GRCh37
NC_000001.9:g.93075667C= NCBI36
NG_011779.1:g.10486C=
NG_033051.1:g.129001G=
NG_011779.2:g.10537C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.594C= (RPL5) MANE Select ENSP00000359345.2:p.His198=
ENST00000645119.1:c.324+2609C= (RPL5) ENSP00000493811.1:n.324+2609C=
ENST00000645300.1:c.444C= (RPL5) ENSP00000495589.1:p.His148=
ENST00000645908.1:n.328C= (RPL5)
ENST00000370321.7:c.594C= (RPL5) ENSP00000359345.2:p.His198=
ENST00000497519.1:n.913C= (RPL5)
ENST00000615519.4:c.475-4488G= (DIPK1A) ENSP00000483279.1:n.475-4488G=
NM_000969.3:c.594C= (RPL5) NP_000960.2:p.His198=
NM_001252273.1:c.475-4488G= (DIPK1A) NP_001239202.1:n.475-4488G=
NM_000969.5:c.594C= (RPL5) MANE Select NP_000960.2:p.His198=
NR_146333.1:n.653C= (RPL5)
NM_001252273.2:c.475-4488G= (DIPK1A) NP_001239202.1:n.475-4488G=