Canonical Allele Identifier: CA341242764

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837460A>C , CM000663.2:g.92837460A>C GRCh38
NC_000001.10:g.93303017A>C , CM000663.1:g.93303017A>C GRCh37
NC_000001.9:g.93075605A>C NCBI36
NG_011779.1:g.10424A>C
NG_033051.1:g.129063T>G
NG_011779.2:g.10475A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.532A>C (RPL5) MANE Select ENSP00000359345.2:p.Lys178Gln
ENST00000645119.1:c.324+2547A>C (RPL5) ENSP00000493811.1:n.324+2547A>C
ENST00000645300.1:c.382A>C (RPL5) ENSP00000495589.1:p.Lys128Gln
ENST00000645908.1:n.266A>C (RPL5)
ENST00000315741.5:c.382A>C (RPL5) ENSP00000359338.2:p.Lys128Gln
ENST00000370321.7:c.532A>C (RPL5) ENSP00000359345.2:p.Lys178Gln
ENST00000497519.1:n.851A>C (RPL5)
ENST00000615519.4:c.475-4426T>G (DIPK1A) ENSP00000483279.1:n.475-4426T>G
NM_000969.3:c.532A>C (RPL5) NP_000960.2:p.Lys178Gln
NM_001252273.1:c.475-4426T>G (DIPK1A) NP_001239202.1:n.475-4426T>G
NM_000969.5:c.532A>C (RPL5) MANE Select NP_000960.2:p.Lys178Gln
NR_146333.1:n.591A>C (RPL5)
NM_001252273.2:c.475-4426T>G (DIPK1A) NP_001239202.1:n.475-4426T>G