Canonical Allele Identifier: CA10556223

Gene: NAA10 ARHGAP4

Linked Data

• ClinVar Variation Id: 1648582
• ClinVar RCV Id: RCV002141267 ; RCV002500324
• dbSNP Id: rs199988253
• ExAC: X:153199376 C / T
• gnomAD v2: X-153199376-C-T
• gnomAD v3: X-153933923-C-T
• gnomAD v4: X-153933923-C-T
• MyVariant Identifiers: chrX:g.153199376C>T (hg19) ; chrX:g.153933923C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153933923C>T , CM000685.2:g.153933923C>T	GRCh38
NC_000023.10:g.153199376C>T , CM000685.1:g.153199376C>T	GRCh37
NC_000023.9:g.152852570C>T	NCBI36
NG_012522.1:g.15857G>A
NG_031987.1:g.6232G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477750.6:n.355+20G>A (NAA10)
ENST00000700299.1:n.297+20G>A (NAA10)
ENST00000464845.6:c.179+20G>A (NAA10) MANE Select	ENSP00000417763.1:n.179+20G>A
ENST00000370009.5:c.179+20G>A (NAA10)	ENSP00000359026.1:n.179+20G>A
ENST00000370011.7:c.161+38G>A (NAA10)	ENSP00000359028.3:n.161+38G>A
ENST00000370015.8:c.179+20G>A (NAA10)	ENSP00000359032.4:n.179+20G>A
ENST00000393710.7:n.290+20G>A (NAA10)
ENST00000393712.7:c.179+20G>A (NAA10)	ENSP00000377315.3:n.179+20G>A
ENST00000432089.1:c.161+38G>A (NAA10)	ENSP00000413668.1:n.161+38G>A
ENST00000460996.5:n.468+20G>A (NAA10)
ENST00000464845.5:c.179+20G>A (NAA10)	ENSP00000417763.1:n.179+20G>A
ENST00000466877.5:n.290+20G>A (NAA10)
ENST00000477750.5:n.355+20G>A (NAA10)
ENST00000478177.1:n.310G>A (NAA10)
ENST00000494813.5:n.274+20G>A (ARHGAP4)
NM_001256119.1:c.179+20G>A (NAA10)	NP_001243048.1:n.179+20G>A
NM_001256120.1:c.161+38G>A (NAA10)	NP_001243049.1:n.161+38G>A
NM_003491.3:c.179+20G>A (NAA10)	NP_003482.1:n.179+20G>A
NM_003491.4:c.179+20G>A (NAA10) MANE Select	NP_003482.1:n.179+20G>A
NM_001256119.2:c.179+20G>A (NAA10)	NP_001243048.1:n.179+20G>A
NM_001256120.2:c.161+38G>A (NAA10)	NP_001243049.1:n.161+38G>A