Canonical Allele Identifier: CA204638
Gene: NAA10 HGNC NCBI
ARHGAP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 208664
ClinVar RCV Id: RCV001257765 RCV002252040 RCV003401042
dbSNP Id: rs797044868
MyVariant Identifiers: chrX:g.153197863G>A (hg19) chrX:g.153932410G>A (hg38)
PubMed: PMID:21700266 PMID:24431331 PMID:25099252 PMID:25489052 PMID:25987439 PMID:26522270 PMID:27094817 PMID:27479843 PMID:28135719 PMID:28967461
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153932410G>A , CM000685.2:g.153932410G>A GRCh38
NC_000023.10:g.153197863G>A , CM000685.1:g.153197863G>A GRCh37
NC_000023.9:g.152851057G>A NCBI36
NG_031987.1:g.7745C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000477750.6:n.423C>T (NAA10)
ENST00000700299.1:n.365C>T (NAA10)
ENST00000464845.6:c.247C>T (NAA10) MANE Select ENSP00000417763.1:p.Arg83Cys
ENST00000370009.5:c.247C>T (NAA10) ENSP00000359026.1:p.Arg83Cys
ENST00000370011.7:c.229C>T (NAA10) ENSP00000359028.3:p.Arg77Cys
ENST00000370015.8:c.247C>T (NAA10) ENSP00000359032.4:p.Arg83Cys
ENST00000393710.7:n.358C>T (NAA10)
ENST00000393712.7:c.247C>T (NAA10) ENSP00000377315.3:p.Arg83Cys
ENST00000432089.1:c.229C>T (NAA10) ENSP00000413668.1:p.Arg77Cys
ENST00000460996.5:n.536C>T (NAA10)
ENST00000464845.5:c.247C>T (NAA10) ENSP00000417763.1:p.Arg83Cys
ENST00000466877.5:n.358C>T (NAA10)
ENST00000477750.5:n.423C>T (NAA10)
ENST00000477882.1:n.466C>T (NAA10)
ENST00000484950.5:n.466C>T (NAA10)
ENST00000494813.5:n.342C>T (ARHGAP4)
NM_001256119.1:c.247C>T (NAA10) NP_001243048.1:p.Arg83Cys
NM_001256120.1:c.229C>T (NAA10) NP_001243049.1:p.Arg77Cys
NM_003491.3:c.247C>T (NAA10) NP_003482.1:p.Arg83Cys
NM_003491.4:c.247C>T (NAA10) MANE Select NP_003482.1:p.Arg83Cys
NM_001256119.2:c.247C>T (NAA10) NP_001243048.1:p.Arg83Cys
NM_001256120.2:c.229C>T (NAA10) NP_001243049.1:p.Arg77Cys
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