Canonical Allele Identifier: CA128774
Gene: NAA10 HGNC NCBI
ARHGAP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 29927
ClinVar RCV Id: RCV000022818
dbSNP Id: rs387906701
MyVariant Identifiers: chrX:g.153199841A>G (hg19) chrX:g.153934388A>G (hg38)
PubMed: PMID:21700266 PMID:25489052
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153934388A>G , CM000685.2:g.153934388A>G GRCh38
NC_000023.10:g.153199841A>G , CM000685.1:g.153199841A>G GRCh37
NC_000023.9:g.152853035A>G NCBI36
NG_012522.1:g.15392T>C
NG_031987.1:g.5767T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000477750.6:n.285T>C (NAA10)
ENST00000700299.1:n.227T>C (NAA10)
ENST00000464845.6:c.109T>C (NAA10) MANE Select ENSP00000417763.1:p.Ser37Pro
ENST00000370009.5:c.109T>C (NAA10) ENSP00000359026.1:p.Ser37Pro
ENST00000370011.7:c.109T>C (NAA10) ENSP00000359028.3:p.Ser37Pro
ENST00000370015.8:c.109T>C (NAA10) ENSP00000359032.4:p.Ser37Pro
ENST00000393710.7:n.220T>C (NAA10)
ENST00000393712.7:c.109T>C (NAA10) ENSP00000377315.3:p.Ser37Pro
ENST00000432089.1:c.109T>C (NAA10) ENSP00000413668.1:p.Ser37Pro
ENST00000460996.5:n.398T>C (NAA10)
ENST00000464845.5:c.109T>C (NAA10) ENSP00000417763.1:p.Ser37Pro
ENST00000466877.5:n.220T>C (NAA10)
ENST00000477750.5:n.285T>C (NAA10)
ENST00000478177.1:n.220T>C (NAA10)
ENST00000488481.1:n.211T>C (NAA10)
ENST00000494813.5:n.204T>C (ARHGAP4)
NM_001256119.1:c.109T>C (NAA10) NP_001243048.1:p.Ser37Pro
NM_001256120.1:c.109T>C (NAA10) NP_001243049.1:p.Ser37Pro
NM_003491.3:c.109T>C (NAA10) NP_003482.1:p.Ser37Pro
NM_003491.4:c.109T>C (NAA10) MANE Select NP_003482.1:p.Ser37Pro
NM_001256119.2:c.109T>C (NAA10) NP_001243048.1:p.Ser37Pro
NM_001256120.2:c.109T>C (NAA10) NP_001243049.1:p.Ser37Pro
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