Canonical Allele Identifier: CA1180933046

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92834917T= , CM000663.2:g.92834917T= GRCh38
NC_000001.10:g.93300474T= , CM000663.1:g.93300474T= GRCh37
NC_000001.9:g.93073062T= NCBI36
NG_011779.1:g.7881T=
NG_033051.1:g.131606A=
NG_011779.2:g.7932T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.324+4T= (RPL5) MANE Select ENSP00000359345.2:n.324+4T=
ENST00000645119.1:c.324+4T= (RPL5) ENSP00000493811.1:n.324+4T=
ENST00000645300.1:c.174+4T= (RPL5) ENSP00000495589.1:n.174+4T=
ENST00000645908.1:n.58+4T= (RPL5)
ENST00000646852.1:n.357T= (RPL5)
ENST00000315741.5:c.174+4T= (RPL5) ENSP00000359338.2:n.174+4T=
ENST00000370321.7:c.324+4T= (RPL5) ENSP00000359345.2:n.324+4T=
ENST00000461952.1:n.1034+4T= (RPL5)
ENST00000470843.5:c.*286+4T= (RPL5) ENSP00000473675.1:n.*286+4T=
ENST00000615519.4:c.475-1883A= (DIPK1A) ENSP00000483279.1:n.475-1883A=
NM_000969.3:c.324+4T= (RPL5) NP_000960.2:n.324+4T=
NM_001252273.1:c.475-1883A= (DIPK1A) NP_001239202.1:n.475-1883A=
NM_000969.5:c.324+4T= (RPL5) MANE Select NP_000960.2:n.324+4T=
NR_146333.1:n.420+37T= (RPL5)
NM_001252273.2:c.475-1883A= (DIPK1A) NP_001239202.1:n.475-1883A=