Canonical Allele Identifier: CA341242792

Linked Data

gnomAD v4: 1-92837472-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837472G>A , CM000663.2:g.92837472G>A GRCh38
NC_000001.10:g.93303029G>A , CM000663.1:g.93303029G>A GRCh37
NC_000001.9:g.93075617G>A NCBI36
NG_011779.1:g.10436G>A
NG_033051.1:g.129051C>T
NG_011779.2:g.10487G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.544G>A (RPL5) MANE Select ENSP00000359345.2:p.Gly182Ser
ENST00000645119.1:c.324+2559G>A (RPL5) ENSP00000493811.1:n.324+2559G>A
ENST00000645300.1:c.394G>A (RPL5) ENSP00000495589.1:p.Gly132Ser
ENST00000645908.1:n.278G>A (RPL5)
ENST00000370321.7:c.544G>A (RPL5) ENSP00000359345.2:p.Gly182Ser
ENST00000497519.1:n.863G>A (RPL5)
ENST00000615519.4:c.475-4438C>T (DIPK1A) ENSP00000483279.1:n.475-4438C>T
NM_000969.3:c.544G>A (RPL5) NP_000960.2:p.Gly182Ser
NM_001252273.1:c.475-4438C>T (DIPK1A) NP_001239202.1:n.475-4438C>T
NM_000969.5:c.544G>A (RPL5) MANE Select NP_000960.2:p.Gly182Ser
NR_146333.1:n.603G>A (RPL5)
NM_001252273.2:c.475-4438C>T (DIPK1A) NP_001239202.1:n.475-4438C>T