Canonical Allele Identifier: CA1148287122

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837547T= , CM000663.2:g.92837547T= GRCh38
NC_000001.10:g.93303104T= , CM000663.1:g.93303104T= GRCh37
NC_000001.9:g.93075692T= NCBI36
NG_011779.1:g.10511T=
NG_033051.1:g.128976A=
NG_011779.2:g.10562T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.619T= (RPL5) MANE Select ENSP00000359345.2:p.Tyr207=
ENST00000645119.1:c.324+2634T= (RPL5) ENSP00000493811.1:n.324+2634T=
ENST00000645300.1:c.469T= (RPL5) ENSP00000495589.1:p.Tyr157=
ENST00000645908.1:n.353T= (RPL5)
ENST00000370321.7:c.619T= (RPL5) ENSP00000359345.2:p.Tyr207=
ENST00000497519.1:n.938T= (RPL5)
ENST00000615519.4:c.475-4513A= (DIPK1A) ENSP00000483279.1:n.475-4513A=
NM_000969.3:c.619T= (RPL5) NP_000960.2:p.Tyr207=
NM_001252273.1:c.475-4513A= (DIPK1A) NP_001239202.1:n.475-4513A=
NM_000969.5:c.619T= (RPL5) MANE Select NP_000960.2:p.Tyr207=
NR_146333.1:n.678T= (RPL5)
NM_001252273.2:c.475-4513A= (DIPK1A) NP_001239202.1:n.475-4513A=