Canonical Allele Identifier: CA524696711

Linked Data

dbSNP Id: rs1200952687
gnomAD v2: 1-93303434-T-G
gnomAD v3: 1-92837877-T-G
gnomAD v4: 1-92837877-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837877T>G , CM000663.2:g.92837877T>G GRCh38
NC_000001.10:g.93303434T>G , CM000663.1:g.93303434T>G GRCh37
NC_000001.9:g.93076022T>G NCBI36
NG_011779.1:g.10841T>G
NG_033051.1:g.128646A>C
NG_011779.2:g.10892T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+244T>G (RPL5) MANE Select ENSP00000359345.2:n.705+244T>G
ENST00000645119.1:c.325-2674T>G (RPL5) ENSP00000493811.1:n.325-2674T>G
ENST00000645300.1:c.555+244T>G (RPL5) ENSP00000495589.1:n.555+244T>G
ENST00000370321.7:c.705+244T>G (RPL5) ENSP00000359345.2:n.705+244T>G
ENST00000497519.1:n.1024+244T>G (RPL5)
ENST00000615519.4:c.475-4843A>C (DIPK1A) ENSP00000483279.1:n.475-4843A>C
NM_000969.3:c.705+244T>G (RPL5) NP_000960.2:n.705+244T>G
NM_001252273.1:c.475-4843A>C (DIPK1A) NP_001239202.1:n.475-4843A>C
NM_000969.5:c.705+244T>G (RPL5) MANE Select NP_000960.2:n.705+244T>G
NR_146333.1:n.764+244T>G (RPL5)
NM_001252273.2:c.475-4843A>C (DIPK1A) NP_001239202.1:n.475-4843A>C