Canonical Allele Identifier: CA2466531268

Gene: NAA10 ARHGAP4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153932073A= , CM000685.2:g.153932073A=	GRCh38
NC_000023.10:g.153197526A= , CM000685.1:g.153197526A=	GRCh37
NC_000023.9:g.152850720A=	NCBI36
NG_031987.1:g.8082T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477750.6:n.760T= (NAA10)
ENST00000700299.1:n.502T= (NAA10)
ENST00000464845.6:c.384T= (NAA10) MANE Select	ENSP00000417763.1:p.Phe128=
ENST00000370009.5:c.341+243T= (NAA10)	ENSP00000359026.1:n.341+243T=
ENST00000370011.7:c.323+243T= (NAA10)	ENSP00000359028.3:n.323+243T=
ENST00000370015.8:c.384T= (NAA10)	ENSP00000359032.4:p.Phe128=
ENST00000393710.7:n.495T= (NAA10)
ENST00000393712.7:c.384T= (NAA10)	ENSP00000377315.3:p.Phe128=
ENST00000432089.1:c.366T= (NAA10)	ENSP00000413668.1:p.Phe122=
ENST00000460996.5:n.673T= (NAA10)
ENST00000464845.5:c.384T= (NAA10)	ENSP00000417763.1:p.Phe128=
ENST00000466877.5:n.695T= (NAA10)
ENST00000467451.1:n.186T= (NAA10)
ENST00000477750.5:n.760T= (NAA10)
ENST00000477882.1:n.803T= (NAA10)
ENST00000484950.5:n.603T= (NAA10)
ENST00000494813.5:n.479T= (ARHGAP4)
NM_001256119.1:c.341+243T= (NAA10)	NP_001243048.1:n.341+243T=
NM_001256120.1:c.366T= (NAA10)	NP_001243049.1:p.Phe122=
NM_003491.3:c.384T= (NAA10)	NP_003482.1:p.Phe128=
NM_003491.4:c.384T= (NAA10) MANE Select	NP_003482.1:p.Phe128=
NM_001256119.2:c.341+243T= (NAA10)	NP_001243048.1:n.341+243T=
NM_001256120.2:c.366T= (NAA10)	NP_001243049.1:p.Phe122=