Canonical Allele Identifier: CA2454712037
Gene: NKAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930230C= , CM000685.2:g.119930230C= GRCh38
NC_000023.10:g.119064193C= , CM000685.1:g.119064193C= GRCh37
NC_000023.9:g.118948221C= NCBI36
NG_021260.1:g.18543G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.924-65G= MANE Select ENSP00000360464.3:n.924-65G=
ENST00000652253.1:c.920-65G=
ENST00000371410.4:c.924-65G= ENSP00000360464.3:n.924-65G=
ENST00000477789.5:n.1852-65G=
ENST00000482407.1:n.723-65G=
NM_024528.3:c.924-65G= NP_078804.2:n.924-65G=
XM_017029842.1:c.627-65G= XP_016885331.1:n.627-65G=
NM_024528.4:c.924-65G= MANE Select NP_078804.2:n.924-65G=