Canonical Allele Identifier: CA2454711977
Gene: NKAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119929912G= , CM000685.2:g.119929912G= GRCh38
NC_000023.10:g.119063875G= , CM000685.1:g.119063875G= GRCh37
NC_000023.9:g.118947903G= NCBI36
NG_021260.1:g.18861C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1073+104C= MANE Select ENSP00000360464.3:n.1073+104C=
ENST00000652253.1:c.1069+104C=
ENST00000371410.4:c.1073+104C= ENSP00000360464.3:n.1073+104C=
ENST00000477789.5:n.2001+104C=
NM_024528.3:c.1073+104C= NP_078804.2:n.1073+104C=
XM_017029842.1:c.776+104C= XP_016885331.1:n.776+104C=
NM_024528.4:c.1073+104C= MANE Select NP_078804.2:n.1073+104C=