Canonical Allele Identifier: CA1180934157

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837484G= , CM000663.2:g.92837484G= GRCh38
NC_000001.10:g.93303041G= , CM000663.1:g.93303041G= GRCh37
NC_000001.9:g.93075629G= NCBI36
NG_011779.1:g.10448G=
NG_033051.1:g.129039C=
NG_011779.2:g.10499G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.556G= (RPL5) MANE Select ENSP00000359345.2:p.Glu186=
ENST00000645119.1:c.324+2571G= (RPL5) ENSP00000493811.1:n.324+2571G=
ENST00000645300.1:c.406G= (RPL5) ENSP00000495589.1:p.Glu136=
ENST00000645908.1:n.290G= (RPL5)
ENST00000370321.7:c.556G= (RPL5) ENSP00000359345.2:p.Glu186=
ENST00000497519.1:n.875G= (RPL5)
ENST00000615519.4:c.475-4450C= (DIPK1A) ENSP00000483279.1:n.475-4450C=
NM_000969.3:c.556G= (RPL5) NP_000960.2:p.Glu186=
NM_001252273.1:c.475-4450C= (DIPK1A) NP_001239202.1:n.475-4450C=
NM_000969.5:c.556G= (RPL5) MANE Select NP_000960.2:p.Glu186=
NR_146333.1:n.615G= (RPL5)
NM_001252273.2:c.475-4450C= (DIPK1A) NP_001239202.1:n.475-4450C=