Canonical Allele Identifier: CA2454712004
Gene: NKAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930042G= , CM000685.2:g.119930042G= GRCh38
NC_000023.10:g.119064005G= , CM000685.1:g.119064005G= GRCh37
NC_000023.9:g.118948033G= NCBI36
NG_021260.1:g.18731C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.1047C= MANE Select ENSP00000360464.3:p.Cys349=
ENST00000652253.1:c.1043C=
ENST00000371410.4:c.1047C= ENSP00000360464.3:p.Cys349=
ENST00000477789.5:n.1975C=
NM_024528.3:c.1047C= NP_078804.2:p.Cys349=
XM_017029842.1:c.750C= XP_016885331.1:p.Cys250=
NM_024528.4:c.1047C= MANE Select NP_078804.2:p.Cys349=