Canonical Allele Identifier: CA341241059
Community Standard Title: NM_000969.5(RPL5):c.170A>G (p.Asn57Ser)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92833641A>G , CM000663.2:g.92833641A>G GRCh38
NC_000001.10:g.93299198A>G , CM000663.1:g.93299198A>G GRCh37
NC_000001.9:g.93071786A>G NCBI36
NG_011779.1:g.6605A>G
NG_033051.1:g.132882T>C
NG_011779.2:g.6656A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000969.5:c.170A>G (RPL5) MANE Select NP_000960.2:p.Asn57Ser
ENST00000370321.8:c.170A>G (RPL5) MANE Select ENSP00000359345.2:p.Asn57Ser
NM_000969.3:c.170A>G (RPL5) NP_000960.2:p.Asn57Ser
NM_001252273.1:c.475-607T>C (DIPK1A) NP_001239202.1:n.475-607T>C
NM_001252273.2:c.475-607T>C (DIPK1A) NP_001239202.1:n.475-607T>C
NR_146333.1:n.299A>G (RPL5)
ENST00000315741.5:c.20A>G (RPL5) ENSP00000359338.2:p.Asn7Ser
ENST00000370321.7:c.170A>G (RPL5) ENSP00000359345.2:p.Asn57Ser
ENST00000461952.1:n.880A>G (RPL5)
ENST00000470843.5:c.170A>G (RPL5) ENSP00000473675.1:p.Asn57Ser
ENST00000615519.4:c.475-607T>C (DIPK1A) ENSP00000483279.1:n.475-607T>C
ENST00000645119.1:c.170A>G (RPL5) ENSP00000493811.1:p.Asn57Ser
ENST00000645300.1:c.20A>G (RPL5) ENSP00000495589.1:p.Asn7Ser
ENST00000646852.1:n.199A>G (RPL5)