Canonical Allele Identifier: CA952528

Linked Data

dbSNP Id: rs775560628
gnomAD v2: 1-93303111-G-A
gnomAD v4: 1-92837554-G-A
COSMIC: COSM913348

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837554G>A , CM000663.2:g.92837554G>A GRCh38
NC_000001.10:g.93303111G>A , CM000663.1:g.93303111G>A GRCh37
NC_000001.9:g.93075699G>A NCBI36
NG_011779.1:g.10518G>A
NG_033051.1:g.128969C>T
NG_011779.2:g.10569G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.626G>A (RPL5) MANE Select ENSP00000359345.2:p.Arg209His
ENST00000645119.1:c.324+2641G>A (RPL5) ENSP00000493811.1:n.324+2641G>A
ENST00000645300.1:c.476G>A (RPL5) ENSP00000495589.1:p.Arg159His
ENST00000645908.1:n.360G>A (RPL5)
ENST00000370321.7:c.626G>A (RPL5) ENSP00000359345.2:p.Arg209His
ENST00000497519.1:n.945G>A (RPL5)
ENST00000615519.4:c.475-4520C>T (DIPK1A) ENSP00000483279.1:n.475-4520C>T
NM_000969.3:c.626G>A (RPL5) NP_000960.2:p.Arg209His
NM_001252273.1:c.475-4520C>T (DIPK1A) NP_001239202.1:n.475-4520C>T
NM_000969.5:c.626G>A (RPL5) MANE Select NP_000960.2:p.Arg209His
NR_146333.1:n.685G>A (RPL5)
NM_001252273.2:c.475-4520C>T (DIPK1A) NP_001239202.1:n.475-4520C>T