Canonical Allele Identifier: CA16043183

Gene: NAA10 ARHGAP4

Linked Data

• ClinVar Variation Id: 373777
• ClinVar RCV Id: RCV000414408 ; RCV000623681
• dbSNP Id: rs1057518605
• MyVariant Identifiers: chrX:g.153196247A>G (hg19) ; chrX:g.153930794A>G (hg38)
• PubMed: PMID:21700266 ; PMID:24431331 ; PMID:25099252 ; PMID:25489052 ; PMID:25987439 ; PMID:26522270 ; PMID:27094817 ; PMID:28967461

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153930794A>G , CM000685.2:g.153930794A>G	GRCh38
NC_000023.10:g.153196247A>G , CM000685.1:g.153196247A>G	GRCh37
NC_000023.9:g.152849441A>G	NCBI36
NG_013220.1:g.468T>C
NG_031987.1:g.9361T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477750.6:n.2039T>C (NAA10)
ENST00000700299.1:n.1692T>C (NAA10)
ENST00000464845.6:c.440T>C (NAA10) MANE Select	ENSP00000417763.1:p.Met147Thr
ENST00000370009.5:c.395T>C (NAA10)	ENSP00000359026.1:p.Met132Thr
ENST00000370011.7:c.377T>C (NAA10)	ENSP00000359028.3:p.Met126Thr
ENST00000370015.8:c.440T>C (NAA10)	ENSP00000359032.4:p.Met147Thr
ENST00000393712.7:c.440T>C (NAA10)	ENSP00000377315.3:p.Met147Thr
ENST00000432089.1:c.422T>C (NAA10)	ENSP00000413668.1:p.Met141Thr
ENST00000460996.5:n.729T>C (NAA10)
ENST00000464845.5:c.440T>C (NAA10)	ENSP00000417763.1:p.Met147Thr
ENST00000466877.5:n.751T>C (NAA10)
ENST00000467451.1:n.242T>C (NAA10)
ENST00000482485.1:n.647T>C (NAA10)
ENST00000484950.5:n.659T>C (NAA10)
ENST00000494813.5:n.481+1277T>C (ARHGAP4)
NM_001256119.1:c.395T>C (NAA10)	NP_001243048.1:p.Met132Thr
NM_001256120.1:c.422T>C (NAA10)	NP_001243049.1:p.Met141Thr
NM_003491.3:c.440T>C (NAA10)	NP_003482.1:p.Met147Thr
NM_003491.4:c.440T>C (NAA10) MANE Select	NP_003482.1:p.Met147Thr
NM_001256119.2:c.395T>C (NAA10)	NP_001243048.1:p.Met132Thr
NM_001256120.2:c.422T>C (NAA10)	NP_001243049.1:p.Met141Thr