Canonical Allele Identifier: CA2454711992
Gene: NKAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119929983T= , CM000685.2:g.119929983T= GRCh38
NC_000023.10:g.119063946T= , CM000685.1:g.119063946T= GRCh37
NC_000023.9:g.118947974T= NCBI36
NG_021260.1:g.18790A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.1073+33A= MANE Select ENSP00000360464.3:n.1073+33A=
ENST00000652253.1:c.1069+33A=
ENST00000371410.4:c.1073+33A= ENSP00000360464.3:n.1073+33A=
ENST00000477789.5:n.2001+33A=
NM_024528.3:c.1073+33A= NP_078804.2:n.1073+33A=
XM_017029842.1:c.776+33A= XP_016885331.1:n.776+33A=
NM_024528.4:c.1073+33A= MANE Select NP_078804.2:n.1073+33A=