Canonical Allele Identifier: CA952343

Linked Data

dbSNP Id: rs778601996
gnomAD v2: 1-93298918-G-A
gnomAD v3: 1-92833361-G-A
gnomAD v4: 1-92833361-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92833361G>A , CM000663.2:g.92833361G>A GRCh38
NC_000001.10:g.93298918G>A , CM000663.1:g.93298918G>A GRCh37
NC_000001.9:g.93071506G>A NCBI36
NG_011779.1:g.6325G>A
NG_033051.1:g.133162C>T
NG_011779.2:g.6376G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370321.8:c.4-28G>A (RPL5) MANE Select ENSP00000359345.2:n.4-28G>A
ENST00000645119.1:c.4-28G>A (RPL5) ENSP00000493811.1:n.4-28G>A
ENST00000645300.1:c.-77-184G>A (RPL5) ENSP00000495589.1:n.-77-184G>A
ENST00000646852.1:n.33-28G>A (RPL5)
ENST00000315741.5:c.-147-28G>A (RPL5) ENSP00000359338.2:n.-147-28G>A
ENST00000370321.7:c.4-28G>A (RPL5) ENSP00000359345.2:n.4-28G>A
ENST00000461952.1:n.600G>A (RPL5)
ENST00000470843.5:c.4-28G>A (RPL5) ENSP00000473675.1:n.4-28G>A
ENST00000615519.4:c.475-327C>T (DIPK1A) ENSP00000483279.1:n.475-327C>T
NM_000969.3:c.4-28G>A (RPL5) NP_000960.2:n.4-28G>A
NM_001252273.1:c.475-327C>T (DIPK1A) NP_001239202.1:n.475-327C>T
NM_000969.5:c.4-28G>A (RPL5) MANE Select NP_000960.2:n.4-28G>A
NR_146333.1:n.133-28G>A (RPL5)
NM_001252273.2:c.475-327C>T (DIPK1A) NP_001239202.1:n.475-327C>T