Canonical Allele Identifier: CA1004467195

Linked Data

dbSNP Id: rs1687187809
gnomAD v3: 1-92837837-G-A
gnomAD v4: 1-92837837-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837837G>A , CM000663.2:g.92837837G>A GRCh38
NC_000001.10:g.93303394G>A , CM000663.1:g.93303394G>A GRCh37
NC_000001.9:g.93075982G>A NCBI36
NG_011779.1:g.10801G>A
NG_033051.1:g.128686C>T
NG_011779.2:g.10852G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+204G>A (RPL5) MANE Select ENSP00000359345.2:n.705+204G>A
ENST00000645119.1:c.325-2714G>A (RPL5) ENSP00000493811.1:n.325-2714G>A
ENST00000645300.1:c.555+204G>A (RPL5) ENSP00000495589.1:n.555+204G>A
ENST00000370321.7:c.705+204G>A (RPL5) ENSP00000359345.2:n.705+204G>A
ENST00000497519.1:n.1024+204G>A (RPL5)
ENST00000615519.4:c.475-4803C>T (DIPK1A) ENSP00000483279.1:n.475-4803C>T
NM_000969.3:c.705+204G>A (RPL5) NP_000960.2:n.705+204G>A
NM_001252273.1:c.475-4803C>T (DIPK1A) NP_001239202.1:n.475-4803C>T
NM_000969.5:c.705+204G>A (RPL5) MANE Select NP_000960.2:n.705+204G>A
NR_146333.1:n.764+204G>A (RPL5)
NM_001252273.2:c.475-4803C>T (DIPK1A) NP_001239202.1:n.475-4803C>T