Canonical Allele Identifier: CA279878
Gene: NAA10 HGNC NCBI
ARHGAP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 218104
ClinVar RCV Id: RCV000202352
dbSNP Id: rs863225427
MyVariant Identifiers: chrX:g.153199447T>G (hg19) chrX:g.153933994T>G (hg38)
PubMed: PMID:26522270
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153933994T>G , CM000685.2:g.153933994T>G GRCh38
NC_000023.10:g.153199447T>G , CM000685.1:g.153199447T>G GRCh37
NC_000023.9:g.152852641T>G NCBI36
NG_012522.1:g.15786A>C
NG_031987.1:g.6161A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000477750.6:n.304A>C (NAA10)
ENST00000700299.1:n.246A>C (NAA10)
ENST00000464845.6:c.128A>C (NAA10) MANE Select ENSP00000417763.1:p.Tyr43Ser
ENST00000370009.5:c.128A>C (NAA10) ENSP00000359026.1:p.Tyr43Ser
ENST00000370011.7:c.128A>C (NAA10) ENSP00000359028.3:p.Tyr43Ser
ENST00000370015.8:c.128A>C (NAA10) ENSP00000359032.4:p.Tyr43Ser
ENST00000393710.7:n.239A>C (NAA10)
ENST00000393712.7:c.128A>C (NAA10) ENSP00000377315.3:p.Tyr43Ser
ENST00000432089.1:c.128A>C (NAA10) ENSP00000413668.1:p.Tyr43Ser
ENST00000460996.5:n.417A>C (NAA10)
ENST00000464845.5:c.128A>C (NAA10) ENSP00000417763.1:p.Tyr43Ser
ENST00000466877.5:n.239A>C (NAA10)
ENST00000477750.5:n.304A>C (NAA10)
ENST00000478177.1:n.239A>C (NAA10)
ENST00000494813.5:n.223A>C (ARHGAP4)
NM_001256119.1:c.128A>C (NAA10) NP_001243048.1:p.Tyr43Ser
NM_001256120.1:c.128A>C (NAA10) NP_001243049.1:p.Tyr43Ser
NM_003491.3:c.128A>C (NAA10) NP_003482.1:p.Tyr43Ser
NM_003491.4:c.128A>C (NAA10) MANE Select NP_003482.1:p.Tyr43Ser
NM_001256119.2:c.128A>C (NAA10) NP_001243048.1:p.Tyr43Ser
NM_001256120.2:c.128A>C (NAA10) NP_001243049.1:p.Tyr43Ser
Search 100 bp 5'
Search 100 bp 3'