Canonical Allele Identifier: CA1180934172

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837526A= , CM000663.2:g.92837526A= GRCh38
NC_000001.10:g.93303083A= , CM000663.1:g.93303083A= GRCh37
NC_000001.9:g.93075671A= NCBI36
NG_011779.1:g.10490A=
NG_033051.1:g.128997T=
NG_011779.2:g.10541A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.598A= (RPL5) MANE Select ENSP00000359345.2:p.Met200=
ENST00000645119.1:c.324+2613A= (RPL5) ENSP00000493811.1:n.324+2613A=
ENST00000645300.1:c.448A= (RPL5) ENSP00000495589.1:p.Met150=
ENST00000645908.1:n.332A= (RPL5)
ENST00000370321.7:c.598A= (RPL5) ENSP00000359345.2:p.Met200=
ENST00000497519.1:n.917A= (RPL5)
ENST00000615519.4:c.475-4492T= (DIPK1A) ENSP00000483279.1:n.475-4492T=
NM_000969.3:c.598A= (RPL5) NP_000960.2:p.Met200=
NM_001252273.1:c.475-4492T= (DIPK1A) NP_001239202.1:n.475-4492T=
NM_000969.5:c.598A= (RPL5) MANE Select NP_000960.2:p.Met200=
NR_146333.1:n.657A= (RPL5)
NM_001252273.2:c.475-4492T= (DIPK1A) NP_001239202.1:n.475-4492T=