Canonical Allele Identifier: CA415158917

Gene: NAA10 ARHGAP4

Linked Data

• ClinVar Variation Id: 520542
• ClinVar RCV Id: RCV000623587
• dbSNP Id: rs1557107528
• MyVariant Identifiers: chrX:g.153197778A>C (hg19) ; chrX:g.153932325A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153932325A>C , CM000685.2:g.153932325A>C	GRCh38
NC_000023.10:g.153197778A>C , CM000685.1:g.153197778A>C	GRCh37
NC_000023.9:g.152850972A>C	NCBI36
NG_031987.1:g.7830T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000477750.6:n.508T>G (NAA10)
ENST00000700299.1:n.450T>G (NAA10)
ENST00000464845.6:c.332T>G (NAA10) MANE Select	ENSP00000417763.1:p.Val111Gly
ENST00000370009.5:c.332T>G (NAA10)	ENSP00000359026.1:p.Val111Gly
ENST00000370011.7:c.314T>G (NAA10)	ENSP00000359028.3:p.Val105Gly
ENST00000370015.8:c.332T>G (NAA10)	ENSP00000359032.4:p.Val111Gly
ENST00000393710.7:n.443T>G (NAA10)
ENST00000393712.7:c.332T>G (NAA10)	ENSP00000377315.3:p.Val111Gly
ENST00000432089.1:c.314T>G (NAA10)	ENSP00000413668.1:p.Val105Gly
ENST00000460996.5:n.621T>G (NAA10)
ENST00000464845.5:c.332T>G (NAA10)	ENSP00000417763.1:p.Val111Gly
ENST00000466877.5:n.443T>G (NAA10)
ENST00000477750.5:n.508T>G (NAA10)
ENST00000477882.1:n.551T>G (NAA10)
ENST00000484950.5:n.551T>G (NAA10)
ENST00000494813.5:n.427T>G (ARHGAP4)
NM_001256119.1:c.332T>G (NAA10)	NP_001243048.1:p.Val111Gly
NM_001256120.1:c.314T>G (NAA10)	NP_001243049.1:p.Val105Gly
NM_003491.3:c.332T>G (NAA10)	NP_003482.1:p.Val111Gly
NM_003491.4:c.332T>G (NAA10) MANE Select	NP_003482.1:p.Val111Gly
NM_001256119.2:c.332T>G (NAA10)	NP_001243048.1:p.Val111Gly
NM_001256120.2:c.314T>G (NAA10)	NP_001243049.1:p.Val105Gly