Canonical Allele Identifier: CA16043233
Gene: NAA10 HGNC NCBI
ARHGAP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 372842
ClinVar RCV Id: RCV000414189
dbSNP Id: rs1057518018

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153932318C>A , CM000685.2:g.153932318C>A GRCh38
NC_000023.10:g.153197771C>A , CM000685.1:g.153197771C>A GRCh37
NC_000023.9:g.152850965C>A NCBI36
NG_031987.1:g.7837G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000477750.6:n.515G>T (NAA10)
ENST00000700299.1:n.457G>T (NAA10)
ENST00000464845.6:c.339G>T (NAA10) MANE Select ENSP00000417763.1:p.Lys113Asn
ENST00000370009.5:c.339G>T (NAA10) ENSP00000359026.1:p.Lys113Asn
ENST00000370011.7:c.321G>T (NAA10) ENSP00000359028.3:p.Lys107Asn
ENST00000370015.8:c.339G>T (NAA10) ENSP00000359032.4:p.Lys113Asn
ENST00000393710.7:n.450G>T (NAA10)
ENST00000393712.7:c.339G>T (NAA10) ENSP00000377315.3:p.Lys113Asn
ENST00000432089.1:c.321G>T (NAA10) ENSP00000413668.1:p.Lys107Asn
ENST00000460996.5:n.628G>T (NAA10)
ENST00000464845.5:c.339G>T (NAA10) ENSP00000417763.1:p.Lys113Asn
ENST00000466877.5:n.450G>T (NAA10)
ENST00000477750.5:n.515G>T (NAA10)
ENST00000477882.1:n.558G>T (NAA10)
ENST00000484950.5:n.558G>T (NAA10)
ENST00000494813.5:n.434G>T (ARHGAP4)
NM_001256119.1:c.339G>T (NAA10) NP_001243048.1:p.Lys113Asn
NM_001256120.1:c.321G>T (NAA10) NP_001243049.1:p.Lys107Asn
NM_003491.3:c.339G>T (NAA10) NP_003482.1:p.Lys113Asn
NM_003491.4:c.339G>T (NAA10) MANE Select NP_003482.1:p.Lys113Asn
NM_001256119.2:c.339G>T (NAA10) NP_001243048.1:p.Lys113Asn
NM_001256120.2:c.321G>T (NAA10) NP_001243049.1:p.Lys107Asn