Canonical Allele Identifier: CA341242979

Linked Data

dbSNP Id: rs1345401244
gnomAD v2: 1-93303109-G-C
gnomAD v3: 1-92837552-G-C
gnomAD v4: 1-92837552-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837552G>C , CM000663.2:g.92837552G>C GRCh38
NC_000001.10:g.93303109G>C , CM000663.1:g.93303109G>C GRCh37
NC_000001.9:g.93075697G>C NCBI36
NG_011779.1:g.10516G>C
NG_033051.1:g.128971C>G
NG_011779.2:g.10567G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.624G>C (RPL5) MANE Select ENSP00000359345.2:p.Met208Ile
ENST00000645119.1:c.324+2639G>C (RPL5) ENSP00000493811.1:n.324+2639G>C
ENST00000645300.1:c.474G>C (RPL5) ENSP00000495589.1:p.Met158Ile
ENST00000645908.1:n.358G>C (RPL5)
ENST00000370321.7:c.624G>C (RPL5) ENSP00000359345.2:p.Met208Ile
ENST00000497519.1:n.943G>C (RPL5)
ENST00000615519.4:c.475-4518C>G (DIPK1A) ENSP00000483279.1:n.475-4518C>G
NM_000969.3:c.624G>C (RPL5) NP_000960.2:p.Met208Ile
NM_001252273.1:c.475-4518C>G (DIPK1A) NP_001239202.1:n.475-4518C>G
NM_000969.5:c.624G>C (RPL5) MANE Select NP_000960.2:p.Met208Ile
NR_146333.1:n.683G>C (RPL5)
NM_001252273.2:c.475-4518C>G (DIPK1A) NP_001239202.1:n.475-4518C>G