Canonical Allele Identifier: CA341242862

Linked Data

dbSNP Id: rs1252688079
gnomAD v3: 1-92837501-T-G
gnomAD v4: 1-92837501-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837501T>G , CM000663.2:g.92837501T>G GRCh38
NC_000001.10:g.93303058T>G , CM000663.1:g.93303058T>G GRCh37
NC_000001.9:g.93075646T>G NCBI36
NG_011779.1:g.10465T>G
NG_033051.1:g.129022A>C
NG_011779.2:g.10516T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.573T>G (RPL5) MANE Select ENSP00000359345.2:p.Asn191Lys
ENST00000645119.1:c.324+2588T>G (RPL5) ENSP00000493811.1:n.324+2588T>G
ENST00000645300.1:c.423T>G (RPL5) ENSP00000495589.1:p.Asn141Lys
ENST00000645908.1:n.307T>G (RPL5)
ENST00000370321.7:c.573T>G (RPL5) ENSP00000359345.2:p.Asn191Lys
ENST00000497519.1:n.892T>G (RPL5)
ENST00000615519.4:c.475-4467A>C (DIPK1A) ENSP00000483279.1:n.475-4467A>C
NM_000969.3:c.573T>G (RPL5) NP_000960.2:p.Asn191Lys
NM_001252273.1:c.475-4467A>C (DIPK1A) NP_001239202.1:n.475-4467A>C
NM_000969.5:c.573T>G (RPL5) MANE Select NP_000960.2:p.Asn191Lys
NR_146333.1:n.632T>G (RPL5)
NM_001252273.2:c.475-4467A>C (DIPK1A) NP_001239202.1:n.475-4467A>C