Canonical Allele Identifier: CA1180933958

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837024T= , CM000663.2:g.92837024T= GRCh38
NC_000001.10:g.93302581T= , CM000663.1:g.93302581T= GRCh37
NC_000001.9:g.93075169T= NCBI36
NG_011779.1:g.9988T=
NG_033051.1:g.129499A=
NG_011779.2:g.10039T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.528-432T= (RPL5) MANE Select ENSP00000359345.2:n.528-432T=
ENST00000645119.1:c.324+2111T= (RPL5) ENSP00000493811.1:n.324+2111T=
ENST00000645300.1:c.378-432T= (RPL5) ENSP00000495589.1:n.378-432T=
ENST00000645908.1:n.262-432T= (RPL5)
ENST00000315741.5:c.378-432T= (RPL5) ENSP00000359338.2:n.378-432T=
ENST00000370321.7:c.528-432T= (RPL5) ENSP00000359345.2:n.528-432T=
ENST00000497519.1:n.415T= (RPL5)
ENST00000615519.4:c.475-3990A= (DIPK1A) ENSP00000483279.1:n.475-3990A=
NM_000969.3:c.528-432T= (RPL5) NP_000960.2:n.528-432T=
NM_001252273.1:c.475-3990A= (DIPK1A) NP_001239202.1:n.475-3990A=
NM_000969.5:c.528-432T= (RPL5) MANE Select NP_000960.2:n.528-432T=
NR_146333.1:n.587-432T= (RPL5)
NM_001252273.2:c.475-3990A= (DIPK1A) NP_001239202.1:n.475-3990A=