Canonical Allele Identifier: CA415159623
Gene: NAA10 HGNC NCBI
ARHGAP4 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_003491.4:c.215T>A (NAA10) MANE Select NP_003482.1:p.Ile72Asn
ENST00000464845.6:c.215T>A (NAA10) MANE Select ENSP00000417763.1:p.Ile72Asn
NM_001256119.1:c.215T>A (NAA10) NP_001243048.1:p.Ile72Asn
NM_001256119.2:c.215T>A (NAA10) NP_001243048.1:p.Ile72Asn
NM_001256120.1:c.197T>A (NAA10) NP_001243049.1:p.Ile66Asn
NM_001256120.2:c.197T>A (NAA10) NP_001243049.1:p.Ile66Asn
NM_003491.3:c.215T>A (NAA10) NP_003482.1:p.Ile72Asn
ENST00000370009.5:c.215T>A (NAA10) ENSP00000359026.1:p.Ile72Asn
ENST00000370011.7:c.197T>A (NAA10) ENSP00000359028.3:p.Ile66Asn
ENST00000370015.8:c.215T>A (NAA10) ENSP00000359032.4:p.Ile72Asn
ENST00000393710.7:n.326T>A (NAA10)
ENST00000393712.7:c.215T>A (NAA10) ENSP00000377315.3:p.Ile72Asn
ENST00000432089.1:c.197T>A (NAA10) ENSP00000413668.1:p.Ile66Asn
ENST00000460996.5:n.504T>A (NAA10)
ENST00000464845.5:c.215T>A (NAA10) ENSP00000417763.1:p.Ile72Asn
ENST00000466877.5:n.326T>A (NAA10)
ENST00000477750.5:n.391T>A (NAA10)
ENST00000477750.6:n.391T>A (NAA10)
ENST00000477882.1:n.434T>A (NAA10)
ENST00000484950.5:n.434T>A (NAA10)
ENST00000494813.5:n.310T>A (ARHGAP4)
ENST00000700299.1:n.333T>A (NAA10)