Canonical Allele Identifier: CA2454711954
Gene: NKAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119929831A= , CM000685.2:g.119929831A= GRCh38
NC_000023.10:g.119063794A= , CM000685.1:g.119063794A= GRCh37
NC_000023.9:g.118947822A= NCBI36
NG_021260.1:g.18942T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.1073+185T= MANE Select ENSP00000360464.3:n.1073+185T=
ENST00000652253.1:c.1069+185T=
ENST00000371410.4:c.1073+185T= ENSP00000360464.3:n.1073+185T=
ENST00000477789.5:n.2001+185T=
NM_024528.3:c.1073+185T= NP_078804.2:n.1073+185T=
XM_017029842.1:c.776+185T= XP_016885331.1:n.776+185T=
NM_024528.4:c.1073+185T= MANE Select NP_078804.2:n.1073+185T=