Canonical Allele Identifier: CA10561712
Gene: RPL10 HGNC NCBI
MyVariant.info:
GRCh38 chrX:g.154398397G>A
GRCh37 chrX:g.153626738G>A
gnomAD v2:
X:153626738 G / A
gnomAD v3:
X:154398397 G / A
gnomAD v4:
chrX-154398397-G-A
Joint Max Group AF 0.33758345 (AFR)
Genomes Max Group AF 0.33591342 (AFR)
Exomes Max Group AF 0.33579567 (AFR)
ClinVar RCV:
RCV001794916
ClinVar Variation:
1327969
dbSNP:
915942
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154398397G>A , CM000685.2:g.154398397G>A GRCh38
NC_000023.10:g.153626738G>A , CM000685.1:g.153626738G>A GRCh37
NC_000023.9:g.153279932G>A NCBI36
NG_012890.2:g.5169G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369817.7:c.-24+3G>A MANE Select ENSP00000358832.2:n.-24+3G>A
ENST00000344746.8:c.-123G>A ENSP00000341730.4:n.-123G>A
ENST00000369817.6:c.-24+3G>A ENSP00000358832.2:n.-24+3G>A
ENST00000424325.6:c.-24+3G>A ENSP00000413436.2:n.-24+3G>A
ENST00000436473.5:c.-25G>A ENSP00000388600.1:n.-25G>A
ENST00000458500.5:c.-24+3G>A ENSP00000395025.1:n.-24+3G>A
ENST00000479366.1:n.446+3G>A
ENST00000482732.1:n.10G>A
ENST00000485196.5:n.19G>A
ENST00000489200.5:n.21G>A
ENST00000491035.5:n.21G>A
ENST00000492572.5:n.348+3G>A
ENST00000618723.4:c.-24+3G>A ENSP00000479103.1:n.-24+3G>A
NM_001256577.2:c.-24+3G>A NP_001243506.2:n.-24+3G>A
NM_001256580.2:c.-24+3G>A NP_001243509.2:n.-24+3G>A
NM_001303624.1:c.-123G>A NP_001290553.1:n.-123G>A
NM_001303625.1:c.-25G>A NP_001290554.1:n.-25G>A
NM_006013.4:c.-24+3G>A NP_006004.3:n.-24+3G>A
NM_001303624.2:c.-123G>A NP_001290553.1:n.-123G>A
NM_006013.5:c.-24+3G>A MANE Select NP_006004.3:n.-24+3G>A
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