Canonical Allele Identifier: CA1149069591

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837473G= , CM000663.2:g.92837473G= GRCh38
NC_000001.10:g.93303030G= , CM000663.1:g.93303030G= GRCh37
NC_000001.9:g.93075618G= NCBI36
NG_011779.1:g.10437G=
NG_033051.1:g.129050C=
NG_011779.2:g.10488G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.545G= (RPL5) MANE Select ENSP00000359345.2:p.Gly182=
ENST00000645119.1:c.324+2560G= (RPL5) ENSP00000493811.1:n.324+2560G=
ENST00000645300.1:c.395G= (RPL5) ENSP00000495589.1:p.Gly132=
ENST00000645908.1:n.279G= (RPL5)
ENST00000370321.7:c.545G= (RPL5) ENSP00000359345.2:p.Gly182=
ENST00000497519.1:n.864G= (RPL5)
ENST00000615519.4:c.475-4439C= (DIPK1A) ENSP00000483279.1:n.475-4439C=
NM_000969.3:c.545G= (RPL5) NP_000960.2:p.Gly182=
NM_001252273.1:c.475-4439C= (DIPK1A) NP_001239202.1:n.475-4439C=
NM_000969.5:c.545G= (RPL5) MANE Select NP_000960.2:p.Gly182=
NR_146333.1:n.604G= (RPL5)
NM_001252273.2:c.475-4439C= (DIPK1A) NP_001239202.1:n.475-4439C=