Canonical Allele Identifier: CA1180933594

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92836121C= , CM000663.2:g.92836121C= GRCh38
NC_000001.10:g.93301678C= , CM000663.1:g.93301678C= GRCh37
NC_000001.9:g.93074266C= NCBI36
NG_011779.1:g.9085C=
NG_033051.1:g.130402G=
NG_011779.2:g.9136C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370321.8:c.325-69C= (RPL5) MANE Select ENSP00000359345.2:n.325-69C=
ENST00000645119.1:c.324+1208C= (RPL5) ENSP00000493811.1:n.324+1208C=
ENST00000645300.1:c.175-69C= (RPL5) ENSP00000495589.1:n.175-69C=
ENST00000645908.1:n.59-69C= (RPL5)
ENST00000315741.5:c.175-69C= (RPL5) ENSP00000359338.2:n.175-69C=
ENST00000370321.7:c.325-69C= (RPL5) ENSP00000359345.2:n.325-69C=
ENST00000461952.1:n.1035-69C= (RPL5)
ENST00000470843.5:c.*287-69C= (RPL5) ENSP00000473675.1:n.*287-69C=
ENST00000615519.4:c.475-3087G= (DIPK1A) ENSP00000483279.1:n.475-3087G=
NM_000969.3:c.325-69C= (RPL5) NP_000960.2:n.325-69C=
NM_001252273.1:c.475-3087G= (DIPK1A) NP_001239202.1:n.475-3087G=
NM_000969.5:c.325-69C= (RPL5) MANE Select NP_000960.2:n.325-69C=
NR_146333.1:n.421-106C= (RPL5)
NM_001252273.2:c.475-3087G= (DIPK1A) NP_001239202.1:n.475-3087G=