Canonical Allele Identifier: CA2454712017
Gene: NKAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930153A= , CM000685.2:g.119930153A= GRCh38
NC_000023.10:g.119064116A= , CM000685.1:g.119064116A= GRCh37
NC_000023.9:g.118948144A= NCBI36
NG_021260.1:g.18620T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.936T= MANE Select ENSP00000360464.3:p.Ala312=
ENST00000652253.1:c.932T=
ENST00000371410.4:c.936T= ENSP00000360464.3:p.Ala312=
ENST00000477789.5:n.1864T=
ENST00000482407.1:n.735T=
NM_024528.3:c.936T= NP_078804.2:p.Ala312=
XM_017029842.1:c.639T= XP_016885331.1:p.Ala213=
NM_024528.4:c.936T= MANE Select NP_078804.2:p.Ala312=