Canonical Allele Identifier: CA2454711965

Gene: NKAP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119929848C= , CM000685.2:g.119929848C=	GRCh38
NC_000023.10:g.119063811C= , CM000685.1:g.119063811C=	GRCh37
NC_000023.9:g.118947839C=	NCBI36
NG_021260.1:g.18925G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371410.5:c.1073+168G= MANE Select	ENSP00000360464.3:n.1073+168G=
ENST00000652253.1:c.1069+168G=
ENST00000371410.4:c.1073+168G=	ENSP00000360464.3:n.1073+168G=
ENST00000477789.5:n.2001+168G=
NM_024528.3:c.1073+168G=	NP_078804.2:n.1073+168G=
XM_017029842.1:c.776+168G=	XP_016885331.1:n.776+168G=
NM_024528.4:c.1073+168G= MANE Select	NP_078804.2:n.1073+168G=