Canonical Allele Identifier: CA952647
Community Standard Title: NM_000969.5(RPL5):c.*1A>G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92841866A>G , CM000663.2:g.92841866A>G GRCh38
NC_000001.10:g.93307423A>G , CM000663.1:g.93307423A>G GRCh37
NC_000001.9:g.93080011A>G NCBI36
NG_011779.1:g.14830A>G
NG_033051.1:g.124657T>C
NG_011779.2:g.14881A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000969.5:c.*1A>G (RPL5) MANE Select NP_000960.2:n.*1A>G
ENST00000370321.8:c.*1A>G (RPL5) MANE Select ENSP00000359345.2:n.*1A>G
NM_000969.3:c.*1A>G (RPL5) NP_000960.2:n.*1A>G
NM_001252273.1:c.474+5317T>C (DIPK1A) NP_001239202.1:n.474+5317T>C
NM_001252273.2:c.474+5317T>C (DIPK1A) NP_001239202.1:n.474+5317T>C
NR_146333.1:n.954A>G (RPL5)
ENST00000370321.7:c.*1A>G (RPL5) ENSP00000359345.2:n.*1A>G
ENST00000615519.4:c.474+5317T>C (DIPK1A) ENSP00000483279.1:n.474+5317T>C
ENST00000644549.1:n.216A>G (RPL5)
ENST00000645119.1:c.*1A>G (RPL5) ENSP00000493811.1:n.*1A>G