Canonical Allele Identifier: CA2466530859

Gene: NAA10 ARHGAP4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153930794A= , CM000685.2:g.153930794A=	GRCh38
NC_000023.10:g.153196247A= , CM000685.1:g.153196247A=	GRCh37
NC_000023.9:g.152849441A=	NCBI36
NG_013220.1:g.468T=
NG_031987.1:g.9361T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477750.6:n.2039T= (NAA10)
ENST00000700299.1:n.1692T= (NAA10)
ENST00000464845.6:c.440T= (NAA10) MANE Select	ENSP00000417763.1:p.Met147=
ENST00000370009.5:c.395T= (NAA10)	ENSP00000359026.1:p.Met132=
ENST00000370011.7:c.377T= (NAA10)	ENSP00000359028.3:p.Met126=
ENST00000370015.8:c.440T= (NAA10)	ENSP00000359032.4:p.Met147=
ENST00000393712.7:c.440T= (NAA10)	ENSP00000377315.3:p.Met147=
ENST00000432089.1:c.422T= (NAA10)	ENSP00000413668.1:p.Met141=
ENST00000460996.5:n.729T= (NAA10)
ENST00000464845.5:c.440T= (NAA10)	ENSP00000417763.1:p.Met147=
ENST00000466877.5:n.751T= (NAA10)
ENST00000467451.1:n.242T= (NAA10)
ENST00000482485.1:n.647T= (NAA10)
ENST00000484950.5:n.659T= (NAA10)
ENST00000494813.5:n.481+1277T= (ARHGAP4)
NM_001256119.1:c.395T= (NAA10)	NP_001243048.1:p.Met132=
NM_001256120.1:c.422T= (NAA10)	NP_001243049.1:p.Met141=
NM_003491.3:c.440T= (NAA10)	NP_003482.1:p.Met147=
NM_003491.4:c.440T= (NAA10) MANE Select	NP_003482.1:p.Met147=
NM_001256119.2:c.395T= (NAA10)	NP_001243048.1:p.Met132=
NM_001256120.2:c.422T= (NAA10)	NP_001243049.1:p.Met141=