Canonical Allele Identifier: CA2695080680

Gene: NAA10 ARHGAP4

Linked Data

• gnomAD v4: X-153931587-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153931587C>A , CM000685.2:g.153931587C>A	GRCh38
NC_000023.10:g.153197040C>A , CM000685.1:g.153197040C>A	GRCh37
NC_000023.9:g.152850234C>A	NCBI36
NG_031987.1:g.8568G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000477750.6:n.1246G>T (NAA10)
ENST00000700299.1:n.899G>T (NAA10)
ENST00000464845.6:c.386+484G>T (NAA10) MANE Select	ENSP00000417763.1:n.386+484G>T
ENST00000370009.5:c.341+729G>T (NAA10)	ENSP00000359026.1:n.341+729G>T
ENST00000370011.7:c.323+729G>T (NAA10)	ENSP00000359028.3:n.323+729G>T
ENST00000370015.8:c.386+484G>T (NAA10)	ENSP00000359032.4:n.386+484G>T
ENST00000393712.7:c.386+484G>T (NAA10)	ENSP00000377315.3:n.386+484G>T
ENST00000432089.1:c.368+484G>T (NAA10)	ENSP00000413668.1:n.368+484G>T
ENST00000460996.5:n.675+484G>T (NAA10)
ENST00000464845.5:c.386+484G>T (NAA10)	ENSP00000417763.1:n.386+484G>T
ENST00000466877.5:n.697+484G>T (NAA10)
ENST00000467451.1:n.188+484G>T (NAA10)
ENST00000484950.5:n.605+484G>T (NAA10)
ENST00000494813.5:n.481+484G>T (ARHGAP4)
NM_001256119.1:c.341+729G>T (NAA10)	NP_001243048.1:n.341+729G>T
NM_001256120.1:c.368+484G>T (NAA10)	NP_001243049.1:n.368+484G>T
NM_003491.3:c.386+484G>T (NAA10)	NP_003482.1:n.386+484G>T
NM_003491.4:c.386+484G>T (NAA10) MANE Select	NP_003482.1:n.386+484G>T
NM_001256119.2:c.341+729G>T (NAA10)	NP_001243048.1:n.341+729G>T
NM_001256120.2:c.368+484G>T (NAA10)	NP_001243049.1:n.368+484G>T