Canonical Allele Identifier: CA10603413

Gene: NAA10 ARHGAP4

Linked Data

• ClinVar Variation Id: 280237
• ClinVar RCV Id: RCV000340214 ; RCV000496143
• dbSNP Id: rs878853263
• MyVariant Identifiers: chrX:g.153197526A>C (hg19) ; chrX:g.153932073A>C (hg38)
• PubMed: PMID:28708303

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153932073A>C , CM000685.2:g.153932073A>C	GRCh38
NC_000023.10:g.153197526A>C , CM000685.1:g.153197526A>C	GRCh37
NC_000023.9:g.152850720A>C	NCBI36
NG_031987.1:g.8082T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000477750.6:n.760T>G (NAA10)
ENST00000700299.1:n.502T>G (NAA10)
ENST00000464845.6:c.384T>G (NAA10) MANE Select	ENSP00000417763.1:p.Phe128Leu
ENST00000370009.5:c.341+243T>G (NAA10)	ENSP00000359026.1:n.341+243T>G
ENST00000370011.7:c.323+243T>G (NAA10)	ENSP00000359028.3:n.323+243T>G
ENST00000370015.8:c.384T>G (NAA10)	ENSP00000359032.4:p.Phe128Leu
ENST00000393710.7:n.495T>G (NAA10)
ENST00000393712.7:c.384T>G (NAA10)	ENSP00000377315.3:p.Phe128Leu
ENST00000432089.1:c.366T>G (NAA10)	ENSP00000413668.1:p.Phe122Leu
ENST00000460996.5:n.673T>G (NAA10)
ENST00000464845.5:c.384T>G (NAA10)	ENSP00000417763.1:p.Phe128Leu
ENST00000466877.5:n.695T>G (NAA10)
ENST00000467451.1:n.186T>G (NAA10)
ENST00000477750.5:n.760T>G (NAA10)
ENST00000477882.1:n.803T>G (NAA10)
ENST00000484950.5:n.603T>G (NAA10)
ENST00000494813.5:n.479T>G (ARHGAP4)
NM_001256119.1:c.341+243T>G (NAA10)	NP_001243048.1:n.341+243T>G
NM_001256120.1:c.366T>G (NAA10)	NP_001243049.1:p.Phe122Leu
NM_003491.3:c.384T>G (NAA10)	NP_003482.1:p.Phe128Leu
NM_003491.4:c.384T>G (NAA10) MANE Select	NP_003482.1:p.Phe128Leu
NM_001256119.2:c.341+243T>G (NAA10)	NP_001243048.1:n.341+243T>G
NM_001256120.2:c.366T>G (NAA10)	NP_001243049.1:p.Phe122Leu