Canonical Allele Identifier: CA341241042
Community Standard Title: NM_000969.5(RPL5):c.161G>C (p.Arg54Pro)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92833632G>C , CM000663.2:g.92833632G>C GRCh38
NC_000001.10:g.93299189G>C , CM000663.1:g.93299189G>C GRCh37
NC_000001.9:g.93071777G>C NCBI36
NG_011779.1:g.6596G>C
NG_033051.1:g.132891C>G
NG_011779.2:g.6647G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000969.5:c.161G>C (RPL5) MANE Select NP_000960.2:p.Arg54Pro
ENST00000370321.8:c.161G>C (RPL5) MANE Select ENSP00000359345.2:p.Arg54Pro
NM_000969.3:c.161G>C (RPL5) NP_000960.2:p.Arg54Pro
NM_001252273.1:c.475-598C>G (DIPK1A) NP_001239202.1:n.475-598C>G
NM_001252273.2:c.475-598C>G (DIPK1A) NP_001239202.1:n.475-598C>G
NR_146333.1:n.290G>C (RPL5)
ENST00000315741.5:c.11G>C (RPL5) ENSP00000359338.2:p.Arg4Pro
ENST00000370321.7:c.161G>C (RPL5) ENSP00000359345.2:p.Arg54Pro
ENST00000461952.1:n.871G>C (RPL5)
ENST00000470843.5:c.161G>C (RPL5) ENSP00000473675.1:p.Arg54Pro
ENST00000615519.4:c.475-598C>G (DIPK1A) ENSP00000483279.1:n.475-598C>G
ENST00000645119.1:c.161G>C (RPL5) ENSP00000493811.1:p.Arg54Pro
ENST00000645300.1:c.11G>C (RPL5) ENSP00000495589.1:p.Arg4Pro
ENST00000646852.1:n.190G>C (RPL5)