Canonical Allele Identifier: CA2466531277

Gene: NAA10 ARHGAP4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153932111G= , CM000685.2:g.153932111G=	GRCh38
NC_000023.10:g.153197564G= , CM000685.1:g.153197564G=	GRCh37
NC_000023.9:g.152850758G=	NCBI36
NG_031987.1:g.8044C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477750.6:n.722C= (NAA10)
ENST00000700299.1:n.464C= (NAA10)
ENST00000464845.6:c.346C= (NAA10) MANE Select	ENSP00000417763.1:p.Arg116=
ENST00000370009.5:c.341+205C= (NAA10)	ENSP00000359026.1:n.341+205C=
ENST00000370011.7:c.323+205C= (NAA10)	ENSP00000359028.3:n.323+205C=
ENST00000370015.8:c.346C= (NAA10)	ENSP00000359032.4:p.Arg116=
ENST00000393710.7:n.457C= (NAA10)
ENST00000393712.7:c.346C= (NAA10)	ENSP00000377315.3:p.Arg116=
ENST00000432089.1:c.328C= (NAA10)	ENSP00000413668.1:p.Arg110=
ENST00000460996.5:n.635C= (NAA10)
ENST00000464845.5:c.346C= (NAA10)	ENSP00000417763.1:p.Arg116=
ENST00000466877.5:n.657C= (NAA10)
ENST00000467451.1:n.148C= (NAA10)
ENST00000477750.5:n.722C= (NAA10)
ENST00000477882.1:n.765C= (NAA10)
ENST00000484950.5:n.565C= (NAA10)
ENST00000494813.5:n.441C= (ARHGAP4)
NM_001256119.1:c.341+205C= (NAA10)	NP_001243048.1:n.341+205C=
NM_001256120.1:c.328C= (NAA10)	NP_001243049.1:p.Arg110=
NM_003491.3:c.346C= (NAA10)	NP_003482.1:p.Arg116=
NM_003491.4:c.346C= (NAA10) MANE Select	NP_003482.1:p.Arg116=
NM_001256119.2:c.341+205C= (NAA10)	NP_001243048.1:n.341+205C=
NM_001256120.2:c.328C= (NAA10)	NP_001243049.1:p.Arg110=