Canonical Allele Identifier: CA524365540
Community Standard Title: NM_000969.5(RPL5):c.3+11G>C
Gene: RPL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92832128G>C , CM000663.2:g.92832128G>C GRCh38
NC_000001.10:g.93297685G>C , CM000663.1:g.93297685G>C GRCh37
NC_000001.9:g.93070273G>C NCBI36
NG_011779.1:g.5092G>C
NG_033051.1:g.134395C>G
NG_011779.2:g.5143G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000969.5:c.3+11G>C MANE Select NP_000960.2:n.3+11G>C
ENST00000370321.8:c.3+11G>C MANE Select ENSP00000359345.2:n.3+11G>C
NM_000969.3:c.3+11G>C NP_000960.2:n.3+11G>C
NR_146333.1:n.132+11G>C
ENST00000315741.5:c.-271G>C ENSP00000359338.2:n.-271G>C
ENST00000370321.7:c.3+11G>C ENSP00000359345.2:n.3+11G>C
ENST00000470843.5:c.3+11G>C ENSP00000473675.1:n.3+11G>C
ENST00000645119.1:c.3+11G>C ENSP00000493811.1:n.3+11G>C
ENST00000645300.1:c.-78+11G>C ENSP00000495589.1:n.-78+11G>C
ENST00000646852.1:n.32+11G>C