Canonical Allele Identifier: CA1180934154

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837477T= , CM000663.2:g.92837477T= GRCh38
NC_000001.10:g.93303034T= , CM000663.1:g.93303034T= GRCh37
NC_000001.9:g.93075622T= NCBI36
NG_011779.1:g.10441T=
NG_033051.1:g.129046A=
NG_011779.2:g.10492T=

Transcript Alleles

HGVS Amino-acid change
ENST00000370321.8:c.549T= (RPL5) MANE Select ENSP00000359345.2:p.Tyr183=
ENST00000645119.1:c.324+2564T= (RPL5) ENSP00000493811.1:n.324+2564T=
ENST00000645300.1:c.399T= (RPL5) ENSP00000495589.1:p.Tyr133=
ENST00000645908.1:n.283T= (RPL5)
ENST00000370321.7:c.549T= (RPL5) ENSP00000359345.2:p.Tyr183=
ENST00000497519.1:n.868T= (RPL5)
ENST00000615519.4:c.475-4443A= (DIPK1A) ENSP00000483279.1:n.475-4443A=
NM_000969.3:c.549T= (RPL5) NP_000960.2:p.Tyr183=
NM_001252273.1:c.475-4443A= (DIPK1A) NP_001239202.1:n.475-4443A=
NM_000969.5:c.549T= (RPL5) MANE Select NP_000960.2:p.Tyr183=
NR_146333.1:n.608T= (RPL5)
NM_001252273.2:c.475-4443A= (DIPK1A) NP_001239202.1:n.475-4443A=