Canonical Allele Identifier: CA1180933598

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92836128T= , CM000663.2:g.92836128T= GRCh38
NC_000001.10:g.93301685T= , CM000663.1:g.93301685T= GRCh37
NC_000001.9:g.93074273T= NCBI36
NG_011779.1:g.9092T=
NG_033051.1:g.130395A=
NG_011779.2:g.9143T=

Transcript Alleles

HGVS Amino-acid change
ENST00000370321.8:c.325-62T= (RPL5) MANE Select ENSP00000359345.2:n.325-62T=
ENST00000645119.1:c.324+1215T= (RPL5) ENSP00000493811.1:n.324+1215T=
ENST00000645300.1:c.175-62T= (RPL5) ENSP00000495589.1:n.175-62T=
ENST00000645908.1:n.59-62T= (RPL5)
ENST00000315741.5:c.175-62T= (RPL5) ENSP00000359338.2:n.175-62T=
ENST00000370321.7:c.325-62T= (RPL5) ENSP00000359345.2:n.325-62T=
ENST00000461952.1:n.1035-62T= (RPL5)
ENST00000470843.5:c.*287-62T= (RPL5) ENSP00000473675.1:n.*287-62T=
ENST00000615519.4:c.475-3094A= (DIPK1A) ENSP00000483279.1:n.475-3094A=
NM_000969.3:c.325-62T= (RPL5) NP_000960.2:n.325-62T=
NM_001252273.1:c.475-3094A= (DIPK1A) NP_001239202.1:n.475-3094A=
NM_000969.5:c.325-62T= (RPL5) MANE Select NP_000960.2:n.325-62T=
NR_146333.1:n.421-99T= (RPL5)
NM_001252273.2:c.475-3094A= (DIPK1A) NP_001239202.1:n.475-3094A=