Canonical Allele Identifier: CA2466531269
Gene: NAA10 HGNC NCBI
ARHGAP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153932075A= , CM000685.2:g.153932075A= GRCh38
NC_000023.10:g.153197528A= , CM000685.1:g.153197528A= GRCh37
NC_000023.9:g.152850722A= NCBI36
NG_031987.1:g.8080T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000477750.6:n.758T= (NAA10)
ENST00000700299.1:n.500T= (NAA10)
ENST00000464845.6:c.382T= (NAA10) MANE Select ENSP00000417763.1:p.Phe128=
ENST00000370009.5:c.341+241T= (NAA10) ENSP00000359026.1:n.341+241T=
ENST00000370011.7:c.323+241T= (NAA10) ENSP00000359028.3:n.323+241T=
ENST00000370015.8:c.382T= (NAA10) ENSP00000359032.4:p.Phe128=
ENST00000393710.7:n.493T= (NAA10)
ENST00000393712.7:c.382T= (NAA10) ENSP00000377315.3:p.Phe128=
ENST00000432089.1:c.364T= (NAA10) ENSP00000413668.1:p.Phe122=
ENST00000460996.5:n.671T= (NAA10)
ENST00000464845.5:c.382T= (NAA10) ENSP00000417763.1:p.Phe128=
ENST00000466877.5:n.693T= (NAA10)
ENST00000467451.1:n.184T= (NAA10)
ENST00000477750.5:n.758T= (NAA10)
ENST00000477882.1:n.801T= (NAA10)
ENST00000484950.5:n.601T= (NAA10)
ENST00000494813.5:n.477T= (ARHGAP4)
NM_001256119.1:c.341+241T= (NAA10) NP_001243048.1:n.341+241T=
NM_001256120.1:c.364T= (NAA10) NP_001243049.1:p.Phe122=
NM_003491.3:c.382T= (NAA10) NP_003482.1:p.Phe128=
NM_003491.4:c.382T= (NAA10) MANE Select NP_003482.1:p.Phe128=
NM_001256119.2:c.341+241T= (NAA10) NP_001243048.1:n.341+241T=
NM_001256120.2:c.364T= (NAA10) NP_001243049.1:p.Phe122=