Canonical Allele Identifier: CA2646597607

Linked Data

gnomAD v4: 1-92837895-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837895G>T , CM000663.2:g.92837895G>T GRCh38
NC_000001.10:g.93303452G>T , CM000663.1:g.93303452G>T GRCh37
NC_000001.9:g.93076040G>T NCBI36
NG_011779.1:g.10859G>T
NG_033051.1:g.128628C>A
NG_011779.2:g.10910G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+262G>T (RPL5) MANE Select ENSP00000359345.2:n.705+262G>T
ENST00000645119.1:c.325-2656G>T (RPL5) ENSP00000493811.1:n.325-2656G>T
ENST00000645300.1:c.555+262G>T (RPL5) ENSP00000495589.1:n.555+262G>T
ENST00000370321.7:c.705+262G>T (RPL5) ENSP00000359345.2:n.705+262G>T
ENST00000497519.1:n.1024+262G>T (RPL5)
ENST00000615519.4:c.475-4861C>A (DIPK1A) ENSP00000483279.1:n.475-4861C>A
NM_000969.3:c.705+262G>T (RPL5) NP_000960.2:n.705+262G>T
NM_001252273.1:c.475-4861C>A (DIPK1A) NP_001239202.1:n.475-4861C>A
NM_000969.5:c.705+262G>T (RPL5) MANE Select NP_000960.2:n.705+262G>T
NR_146333.1:n.764+262G>T (RPL5)
NM_001252273.2:c.475-4861C>A (DIPK1A) NP_001239202.1:n.475-4861C>A