Canonical Allele Identifier: CA2454711976
Gene: NKAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119929906_119929907delinsTC , CM000685.2:g.119929906_119929907delinsTC GRCh38
NC_000023.10:g.119063869_119063870delinsTC , CM000685.1:g.119063869_119063870delinsTC GRCh37
NC_000023.9:g.118947897_118947898delinsTC NCBI36
NG_021260.1:g.18866_18867delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1073+109_1073+110delinsGA MANE Select ENSP00000360464.3:n.1073+109_1073+110deli...
ENST00000652253.1:c.1069+109_1069+110delinsGA
ENST00000371410.4:c.1073+109_1073+110delinsGA ENSP00000360464.3:n.1073+109_1073+110deli...
ENST00000477789.5:n.2001+109_2001+110delinsGA
NM_024528.3:c.1073+109_1073+110delinsGA NP_078804.2:n.1073+109_1073+110delinsGA
XM_017029842.1:c.776+109_776+110delinsGA XP_016885331.1:n.776+109_776+110delinsGA
NM_024528.4:c.1073+109_1073+110delinsGA MANE Select NP_078804.2:n.1073+109_1073+110delinsGA