Canonical Allele Identifier: CA2454712014
Gene: NKAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930129A= , CM000685.2:g.119930129A= GRCh38
NC_000023.10:g.119064092A= , CM000685.1:g.119064092A= GRCh37
NC_000023.9:g.118948120A= NCBI36
NG_021260.1:g.18644T=

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.960T= MANE Select ENSP00000360464.3:p.Ala320=
ENST00000652253.1:c.956T=
ENST00000371410.4:c.960T= ENSP00000360464.3:p.Ala320=
ENST00000477789.5:n.1888T=
ENST00000482407.1:n.759T=
NM_024528.3:c.960T= NP_078804.2:p.Ala320=
XM_017029842.1:c.663T= XP_016885331.1:p.Ala221=
NM_024528.4:c.960T= MANE Select NP_078804.2:p.Ala320=