Canonical Allele Identifier: CA341242782

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837468C>A , CM000663.2:g.92837468C>A GRCh38
NC_000001.10:g.93303025C>A , CM000663.1:g.93303025C>A GRCh37
NC_000001.9:g.93075613C>A NCBI36
NG_011779.1:g.10432C>A
NG_033051.1:g.129055G>T
NG_011779.2:g.10483C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370321.8:c.540C>A (RPL5) MANE Select ENSP00000359345.2:p.Phe180Leu
ENST00000645119.1:c.324+2555C>A (RPL5) ENSP00000493811.1:n.324+2555C>A
ENST00000645300.1:c.390C>A (RPL5) ENSP00000495589.1:p.Phe130Leu
ENST00000645908.1:n.274C>A (RPL5)
ENST00000315741.5:c.390C>A (RPL5) ENSP00000359338.2:p.Phe130Leu
ENST00000370321.7:c.540C>A (RPL5) ENSP00000359345.2:p.Phe180Leu
ENST00000497519.1:n.859C>A (RPL5)
ENST00000615519.4:c.475-4434G>T (DIPK1A) ENSP00000483279.1:n.475-4434G>T
NM_000969.3:c.540C>A (RPL5) NP_000960.2:p.Phe180Leu
NM_001252273.1:c.475-4434G>T (DIPK1A) NP_001239202.1:n.475-4434G>T
NM_000969.5:c.540C>A (RPL5) MANE Select NP_000960.2:p.Phe180Leu
NR_146333.1:n.599C>A (RPL5)
NM_001252273.2:c.475-4434G>T (DIPK1A) NP_001239202.1:n.475-4434G>T