Canonical Allele Identifier: CA341240898

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92833589G>A , CM000663.2:g.92833589G>A GRCh38
NC_000001.10:g.93299146G>A , CM000663.1:g.93299146G>A GRCh37
NC_000001.9:g.93071734G>A NCBI36
NG_011779.1:g.6553G>A
NG_033051.1:g.132934C>T
NG_011779.2:g.6604G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.118G>A (RPL5) MANE Select ENSP00000359345.2:p.Asp40Asn
ENST00000645119.1:c.118G>A (RPL5) ENSP00000493811.1:p.Asp40Asn
ENST00000645300.1:c.-33G>A (RPL5) ENSP00000495589.1:n.-33G>A
ENST00000646852.1:n.147G>A (RPL5)
ENST00000315741.5:c.-33G>A (RPL5) ENSP00000359338.2:n.-33G>A
ENST00000370321.7:c.118G>A (RPL5) ENSP00000359345.2:p.Asp40Asn
ENST00000461952.1:n.828G>A (RPL5)
ENST00000470843.5:c.118G>A (RPL5) ENSP00000473675.1:p.Asp40Asn
ENST00000615519.4:c.475-555C>T (DIPK1A) ENSP00000483279.1:n.475-555C>T
NM_000969.3:c.118G>A (RPL5) NP_000960.2:p.Asp40Asn
NM_001252273.1:c.475-555C>T (DIPK1A) NP_001239202.1:n.475-555C>T
NM_000969.5:c.118G>A (RPL5) MANE Select NP_000960.2:p.Asp40Asn
NR_146333.1:n.247G>A (RPL5)
NM_001252273.2:c.475-555C>T (DIPK1A) NP_001239202.1:n.475-555C>T