Canonical Allele Identifier: CA341242762

Linked Data

gnomAD v4: 1-92837458-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837458C>G , CM000663.2:g.92837458C>G GRCh38
NC_000001.10:g.93303015C>G , CM000663.1:g.93303015C>G GRCh37
NC_000001.9:g.93075603C>G NCBI36
NG_011779.1:g.10422C>G
NG_033051.1:g.129065G>C
NG_011779.2:g.10473C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.530C>G (RPL5) MANE Select ENSP00000359345.2:p.Thr177Ser
ENST00000645119.1:c.324+2545C>G (RPL5) ENSP00000493811.1:n.324+2545C>G
ENST00000645300.1:c.380C>G (RPL5) ENSP00000495589.1:p.Thr127Ser
ENST00000645908.1:n.264C>G (RPL5)
ENST00000315741.5:c.380C>G (RPL5) ENSP00000359338.2:p.Thr127Ser
ENST00000370321.7:c.530C>G (RPL5) ENSP00000359345.2:p.Thr177Ser
ENST00000497519.1:n.849C>G (RPL5)
ENST00000615519.4:c.475-4424G>C (DIPK1A) ENSP00000483279.1:n.475-4424G>C
NM_000969.3:c.530C>G (RPL5) NP_000960.2:p.Thr177Ser
NM_001252273.1:c.475-4424G>C (DIPK1A) NP_001239202.1:n.475-4424G>C
NM_000969.5:c.530C>G (RPL5) MANE Select NP_000960.2:p.Thr177Ser
NR_146333.1:n.589C>G (RPL5)
NM_001252273.2:c.475-4424G>C (DIPK1A) NP_001239202.1:n.475-4424G>C