Canonical Allele Identifier: CA1180932389

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92833377T= , CM000663.2:g.92833377T= GRCh38
NC_000001.10:g.93298934T= , CM000663.1:g.93298934T= GRCh37
NC_000001.9:g.93071522T= NCBI36
NG_011779.1:g.6341T=
NG_033051.1:g.133146A=
NG_011779.2:g.6392T=

Transcript Alleles

HGVS Amino-acid change
ENST00000370321.8:c.4-12T= (RPL5) MANE Select ENSP00000359345.2:n.4-12T=
ENST00000645119.1:c.4-12T= (RPL5) ENSP00000493811.1:n.4-12T=
ENST00000645300.1:c.-77-168T= (RPL5) ENSP00000495589.1:n.-77-168T=
ENST00000646852.1:n.33-12T= (RPL5)
ENST00000315741.5:c.-147-12T= (RPL5) ENSP00000359338.2:n.-147-12T=
ENST00000370321.7:c.4-12T= (RPL5) ENSP00000359345.2:n.4-12T=
ENST00000461952.1:n.616T= (RPL5)
ENST00000470843.5:c.4-12T= (RPL5) ENSP00000473675.1:n.4-12T=
ENST00000615519.4:c.475-343A= (DIPK1A) ENSP00000483279.1:n.475-343A=
NM_000969.3:c.4-12T= (RPL5) NP_000960.2:n.4-12T=
NM_001252273.1:c.475-343A= (DIPK1A) NP_001239202.1:n.475-343A=
NM_000969.5:c.4-12T= (RPL5) MANE Select NP_000960.2:n.4-12T=
NR_146333.1:n.133-12T= (RPL5)
NM_001252273.2:c.475-343A= (DIPK1A) NP_001239202.1:n.475-343A=