Canonical Allele Identifier: CA2586966845

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837502dup , CM000663.2:g.92837502dup GRCh38
NC_000001.10:g.93303059dup , CM000663.1:g.93303059dup GRCh37
NC_000001.9:g.93075647dup NCBI36
NG_011779.1:g.10466dup
NG_033051.1:g.129021dup
NG_011779.2:g.10517dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.574dup (RPL5) MANE Select ENSP00000359345.2:p.Ala192GlyfsTer25
ENST00000645119.1:c.324+2589dup (RPL5) ENSP00000493811.1:n.324+2589dup
ENST00000645300.1:c.424dup (RPL5) ENSP00000495589.1:p.Ala142GlyfsTer25
ENST00000645908.1:n.308dup (RPL5)
ENST00000370321.7:c.574dup (RPL5) ENSP00000359345.2:p.Ala192GlyfsTer25
ENST00000497519.1:n.893dup (RPL5)
ENST00000615519.4:c.475-4468dup (DIPK1A) ENSP00000483279.1:n.475-4468dup
NM_000969.3:c.574dup (RPL5) NP_000960.2:p.Ala192GlyfsTer25
NM_001252273.1:c.475-4468dup (DIPK1A) NP_001239202.1:n.475-4468dup
NM_000969.5:c.574dup (RPL5) MANE Select NP_000960.2:p.Ala192GlyfsTer25
NR_146333.1:n.633dup (RPL5)
NM_001252273.2:c.475-4468dup (DIPK1A) NP_001239202.1:n.475-4468dup