Canonical Allele Identifier: CA658656945

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92834845dup , CM000663.2:g.92834845dup GRCh38
NC_000001.10:g.93300402dup , CM000663.1:g.93300402dup GRCh37
NC_000001.9:g.93072990dup NCBI36
NG_011779.1:g.7809dup
NG_033051.1:g.131678dup
NG_011779.2:g.7860dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.256dup (RPL5) MANE Select ENSP00000359345.2:p.Tyr86LeufsTer27
ENST00000645119.1:c.256dup (RPL5) ENSP00000493811.1:p.Tyr86LeufsTer29
ENST00000645300.1:c.106dup (RPL5) ENSP00000495589.1:p.Tyr36LeufsTer27
ENST00000646852.1:n.285dup (RPL5)
ENST00000315741.5:c.106dup (RPL5) ENSP00000359338.2:p.Tyr36LeufsTer27
ENST00000370321.7:c.256dup (RPL5) ENSP00000359345.2:p.Tyr86LeufsTer27
ENST00000461952.1:n.966dup (RPL5)
ENST00000470843.5:c.*218dup (RPL5) ENSP00000473675.1:n.*218dup
ENST00000615519.4:c.475-1811dup (DIPK1A) ENSP00000483279.1:n.475-1811dup
NM_000969.3:c.256dup (RPL5) NP_000960.2:p.Tyr86LeufsTer27
NM_001252273.1:c.475-1811dup (DIPK1A) NP_001239202.1:n.475-1811dup
NM_000969.5:c.256dup (RPL5) MANE Select NP_000960.2:p.Tyr86LeufsTer27
NR_146333.1:n.385dup (RPL5)
NM_001252273.2:c.475-1811dup (DIPK1A) NP_001239202.1:n.475-1811dup