Canonical Allele Identifier: CA341242775

Linked Data

gnomAD v4: 1-92837464-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837464G>C , CM000663.2:g.92837464G>C GRCh38
NC_000001.10:g.93303021G>C , CM000663.1:g.93303021G>C GRCh37
NC_000001.9:g.93075609G>C NCBI36
NG_011779.1:g.10428G>C
NG_033051.1:g.129059C>G
NG_011779.2:g.10479G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370321.8:c.536G>C (RPL5) MANE Select ENSP00000359345.2:p.Arg179Pro
ENST00000645119.1:c.324+2551G>C (RPL5) ENSP00000493811.1:n.324+2551G>C
ENST00000645300.1:c.386G>C (RPL5) ENSP00000495589.1:p.Arg129Pro
ENST00000645908.1:n.270G>C (RPL5)
ENST00000315741.5:c.386G>C (RPL5) ENSP00000359338.2:p.Arg129Pro
ENST00000370321.7:c.536G>C (RPL5) ENSP00000359345.2:p.Arg179Pro
ENST00000497519.1:n.855G>C (RPL5)
ENST00000615519.4:c.475-4430C>G (DIPK1A) ENSP00000483279.1:n.475-4430C>G
NM_000969.3:c.536G>C (RPL5) NP_000960.2:p.Arg179Pro
NM_001252273.1:c.475-4430C>G (DIPK1A) NP_001239202.1:n.475-4430C>G
NM_000969.5:c.536G>C (RPL5) MANE Select NP_000960.2:p.Arg179Pro
NR_146333.1:n.595G>C (RPL5)
NM_001252273.2:c.475-4430C>G (DIPK1A) NP_001239202.1:n.475-4430C>G