Canonical Allele Identifier: CA2454711996
Gene: NKAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930003G= , CM000685.2:g.119930003G= GRCh38
NC_000023.10:g.119063966G= , CM000685.1:g.119063966G= GRCh37
NC_000023.9:g.118947994G= NCBI36
NG_021260.1:g.18770C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1073+13C= MANE Select ENSP00000360464.3:n.1073+13C=
ENST00000652253.1:c.1069+13C=
ENST00000371410.4:c.1073+13C= ENSP00000360464.3:n.1073+13C=
ENST00000477789.5:n.2001+13C=
NM_024528.3:c.1073+13C= NP_078804.2:n.1073+13C=
XM_017029842.1:c.776+13C= XP_016885331.1:n.776+13C=
NM_024528.4:c.1073+13C= MANE Select NP_078804.2:n.1073+13C=