Canonical Allele Identifier: CA2466531112
Gene: NAA10 HGNC NCBI
ARHGAP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153931605C= , CM000685.2:g.153931605C= GRCh38
NC_000023.10:g.153197058C= , CM000685.1:g.153197058C= GRCh37
NC_000023.9:g.152850252C= NCBI36
NG_031987.1:g.8550G=

Transcript Alleles

HGVS Amino-acid change
ENST00000477750.6:n.1228G= (NAA10)
ENST00000700299.1:n.881G= (NAA10)
ENST00000464845.6:c.386+466G= (NAA10) MANE Select ENSP00000417763.1:n.386+466G=
ENST00000370009.5:c.341+711G= (NAA10) ENSP00000359026.1:n.341+711G=
ENST00000370011.7:c.323+711G= (NAA10) ENSP00000359028.3:n.323+711G=
ENST00000370015.8:c.386+466G= (NAA10) ENSP00000359032.4:n.386+466G=
ENST00000393712.7:c.386+466G= (NAA10) ENSP00000377315.3:n.386+466G=
ENST00000432089.1:c.368+466G= (NAA10) ENSP00000413668.1:n.368+466G=
ENST00000460996.5:n.675+466G= (NAA10)
ENST00000464845.5:c.386+466G= (NAA10) ENSP00000417763.1:n.386+466G=
ENST00000466877.5:n.697+466G= (NAA10)
ENST00000467451.1:n.188+466G= (NAA10)
ENST00000484950.5:n.605+466G= (NAA10)
ENST00000494813.5:n.481+466G= (ARHGAP4)
NM_001256119.1:c.341+711G= (NAA10) NP_001243048.1:n.341+711G=
NM_001256120.1:c.368+466G= (NAA10) NP_001243049.1:n.368+466G=
NM_003491.3:c.386+466G= (NAA10) NP_003482.1:n.386+466G=
NM_003491.4:c.386+466G= (NAA10) MANE Select NP_003482.1:n.386+466G=
NM_001256119.2:c.341+711G= (NAA10) NP_001243048.1:n.341+711G=
NM_001256120.2:c.368+466G= (NAA10) NP_001243049.1:n.368+466G=