Canonical Allele Identifier: CA26762445
Community Standard Title: NM_000969.5(RPL5):c.807C>A (p.Pro269=)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92841778C>A , CM000663.2:g.92841778C>A GRCh38
NC_000001.10:g.93307335C>A , CM000663.1:g.93307335C>A GRCh37
NC_000001.9:g.93079923C>A NCBI36
NG_011779.1:g.14742C>A
NG_033051.1:g.124745G>T
NG_011779.2:g.14793C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000969.5:c.807C>A (RPL5) MANE Select NP_000960.2:p.Pro269=
ENST00000370321.8:c.807C>A (RPL5) MANE Select ENSP00000359345.2:p.Pro269=
NM_000969.3:c.807C>A (RPL5) NP_000960.2:p.Pro269=
NM_001252273.1:c.474+5405G>T (DIPK1A) NP_001239202.1:n.474+5405G>T
NM_001252273.2:c.474+5405G>T (DIPK1A) NP_001239202.1:n.474+5405G>T
NR_146333.1:n.866C>A (RPL5)
ENST00000370321.7:c.807C>A (RPL5) ENSP00000359345.2:p.Pro269=
ENST00000497519.1:n.1126C>A (RPL5)
ENST00000615519.4:c.474+5405G>T (DIPK1A) ENSP00000483279.1:n.474+5405G>T
ENST00000644549.1:n.128C>A (RPL5)
ENST00000645119.1:c.426C>A (RPL5) ENSP00000493811.1:p.Pro142=
ENST00000645300.1:c.657C>A (RPL5) ENSP00000495589.1:p.Pro219=