Canonical Allele Identifier: CA418789325

Linked Data

gnomAD v4: 1-92837492-G-A
MyVariant Identifiers: chr1:g.93303049G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837492G>A , CM000663.2:g.92837492G>A GRCh38
NC_000001.10:g.93303049G>A , CM000663.1:g.93303049G>A GRCh37
NC_000001.9:g.93075637G>A NCBI36
NG_011779.1:g.10456G>A
NG_033051.1:g.129031C>T
NG_011779.2:g.10507G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.564G>A (RPL5) MANE Select ENSP00000359345.2:p.Lys188=
ENST00000645119.1:c.324+2579G>A (RPL5) ENSP00000493811.1:n.324+2579G>A
ENST00000645300.1:c.414G>A (RPL5) ENSP00000495589.1:p.Lys138=
ENST00000645908.1:n.298G>A (RPL5)
ENST00000370321.7:c.564G>A (RPL5) ENSP00000359345.2:p.Lys188=
ENST00000497519.1:n.883G>A (RPL5)
ENST00000615519.4:c.475-4458C>T (DIPK1A) ENSP00000483279.1:n.475-4458C>T
NM_000969.3:c.564G>A (RPL5) NP_000960.2:p.Lys188=
NM_001252273.1:c.475-4458C>T (DIPK1A) NP_001239202.1:n.475-4458C>T
NM_000969.5:c.564G>A (RPL5) MANE Select NP_000960.2:p.Lys188=
NR_146333.1:n.623G>A (RPL5)
NM_001252273.2:c.475-4458C>T (DIPK1A) NP_001239202.1:n.475-4458C>T