Canonical Allele Identifier: CA2454712018

Gene: NKAP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119930156A= , CM000685.2:g.119930156A=	GRCh38
NC_000023.10:g.119064119A= , CM000685.1:g.119064119A=	GRCh37
NC_000023.9:g.118948147A=	NCBI36
NG_021260.1:g.18617T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371410.5:c.933T= MANE Select	ENSP00000360464.3:p.His311=
ENST00000652253.1:c.929T=
ENST00000371410.4:c.933T=	ENSP00000360464.3:p.His311=
ENST00000477789.5:n.1861T=
ENST00000482407.1:n.732T=
NM_024528.3:c.933T=	NP_078804.2:p.His311=
XM_017029842.1:c.636T=	XP_016885331.1:p.His212=
NM_024528.4:c.933T= MANE Select	NP_078804.2:p.His311=