Canonical Allele Identifier: CA341242781

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837467T>G , CM000663.2:g.92837467T>G GRCh38
NC_000001.10:g.93303024T>G , CM000663.1:g.93303024T>G GRCh37
NC_000001.9:g.93075612T>G NCBI36
NG_011779.1:g.10431T>G
NG_033051.1:g.129056A>C
NG_011779.2:g.10482T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370321.8:c.539T>G (RPL5) MANE Select ENSP00000359345.2:p.Phe180Cys
ENST00000645119.1:c.324+2554T>G (RPL5) ENSP00000493811.1:n.324+2554T>G
ENST00000645300.1:c.389T>G (RPL5) ENSP00000495589.1:p.Phe130Cys
ENST00000645908.1:n.273T>G (RPL5)
ENST00000315741.5:c.389T>G (RPL5) ENSP00000359338.2:p.Phe130Cys
ENST00000370321.7:c.539T>G (RPL5) ENSP00000359345.2:p.Phe180Cys
ENST00000497519.1:n.858T>G (RPL5)
ENST00000615519.4:c.475-4433A>C (DIPK1A) ENSP00000483279.1:n.475-4433A>C
NM_000969.3:c.539T>G (RPL5) NP_000960.2:p.Phe180Cys
NM_001252273.1:c.475-4433A>C (DIPK1A) NP_001239202.1:n.475-4433A>C
NM_000969.5:c.539T>G (RPL5) MANE Select NP_000960.2:p.Phe180Cys
NR_146333.1:n.598T>G (RPL5)
NM_001252273.2:c.475-4433A>C (DIPK1A) NP_001239202.1:n.475-4433A>C