Canonical Allele Identifier: CA341241434

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92834778G>A , CM000663.2:g.92834778G>A GRCh38
NC_000001.10:g.93300335G>A , CM000663.1:g.93300335G>A GRCh37
NC_000001.9:g.93072923G>A NCBI36
NG_011779.1:g.7742G>A
NG_033051.1:g.131745C>T
NG_011779.2:g.7793G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.190-1G>A (RPL5) MANE Select ENSP00000359345.2:n.190-1G>A
ENST00000645119.1:c.190-1G>A (RPL5) ENSP00000493811.1:n.190-1G>A
ENST00000645300.1:c.40-1G>A (RPL5) ENSP00000495589.1:n.40-1G>A
ENST00000646852.1:n.219-1G>A (RPL5)
ENST00000315741.5:c.40-1G>A (RPL5) ENSP00000359338.2:n.40-1G>A
ENST00000370321.7:c.190-1G>A (RPL5) ENSP00000359345.2:n.190-1G>A
ENST00000461952.1:n.900-1G>A (RPL5)
ENST00000470843.5:c.*152-1G>A (RPL5) ENSP00000473675.1:n.*152-1G>A
ENST00000615519.4:c.475-1744C>T (DIPK1A) ENSP00000483279.1:n.475-1744C>T
NM_000969.3:c.190-1G>A (RPL5) NP_000960.2:n.190-1G>A
NM_001252273.1:c.475-1744C>T (DIPK1A) NP_001239202.1:n.475-1744C>T
NM_000969.5:c.190-1G>A (RPL5) MANE Select NP_000960.2:n.190-1G>A
NR_146333.1:n.319-1G>A (RPL5)
NM_001252273.2:c.475-1744C>T (DIPK1A) NP_001239202.1:n.475-1744C>T