Canonical Allele Identifier: CA16044240

Gene: NAA10 ARHGAP4

Linked Data

• ClinVar Variation Id: 375388
• ClinVar RCV Id: RCV000416440 ; RCV003493567
• dbSNP Id: rs1057519448
• MyVariant Identifiers: chrX:g.153198002A>G (hg19) ; chrX:g.153932549A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153932549A>G , CM000685.2:g.153932549A>G	GRCh38
NC_000023.10:g.153198002A>G , CM000685.1:g.153198002A>G	GRCh37
NC_000023.9:g.152851196A>G	NCBI36
NG_031987.1:g.7606T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477750.6:n.391T>C (NAA10)
ENST00000700299.1:n.333T>C (NAA10)
ENST00000464845.6:c.215T>C (NAA10) MANE Select	ENSP00000417763.1:p.Ile72Thr
ENST00000370009.5:c.215T>C (NAA10)	ENSP00000359026.1:p.Ile72Thr
ENST00000370011.7:c.197T>C (NAA10)	ENSP00000359028.3:p.Ile66Thr
ENST00000370015.8:c.215T>C (NAA10)	ENSP00000359032.4:p.Ile72Thr
ENST00000393710.7:n.326T>C (NAA10)
ENST00000393712.7:c.215T>C (NAA10)	ENSP00000377315.3:p.Ile72Thr
ENST00000432089.1:c.197T>C (NAA10)	ENSP00000413668.1:p.Ile66Thr
ENST00000460996.5:n.504T>C (NAA10)
ENST00000464845.5:c.215T>C (NAA10)	ENSP00000417763.1:p.Ile72Thr
ENST00000466877.5:n.326T>C (NAA10)
ENST00000477750.5:n.391T>C (NAA10)
ENST00000477882.1:n.434T>C (NAA10)
ENST00000484950.5:n.434T>C (NAA10)
ENST00000494813.5:n.310T>C (ARHGAP4)
NM_001256119.1:c.215T>C (NAA10)	NP_001243048.1:p.Ile72Thr
NM_001256120.1:c.197T>C (NAA10)	NP_001243049.1:p.Ile66Thr
NM_003491.3:c.215T>C (NAA10)	NP_003482.1:p.Ile72Thr
NM_003491.4:c.215T>C (NAA10) MANE Select	NP_003482.1:p.Ile72Thr
NM_001256119.2:c.215T>C (NAA10)	NP_001243048.1:p.Ile72Thr
NM_001256120.2:c.197T>C (NAA10)	NP_001243049.1:p.Ile66Thr