Canonical Allele Identifier: CA2454712019

Gene: NKAP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119930172A= , CM000685.2:g.119930172A=	GRCh38
NC_000023.10:g.119064135A= , CM000685.1:g.119064135A=	GRCh37
NC_000023.9:g.118948163A=	NCBI36
NG_021260.1:g.18601T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371410.5:c.924-7T= MANE Select	ENSP00000360464.3:n.924-7T=
ENST00000652253.1:c.920-7T=
ENST00000371410.4:c.924-7T=	ENSP00000360464.3:n.924-7T=
ENST00000477789.5:n.1852-7T=
ENST00000482407.1:n.723-7T=
NM_024528.3:c.924-7T=	NP_078804.2:n.924-7T=
XM_017029842.1:c.627-7T=	XP_016885331.1:n.627-7T=
NM_024528.4:c.924-7T= MANE Select	NP_078804.2:n.924-7T=