Canonical Allele Identifier: CA2454711950

Gene: NKAP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119929825A= , CM000685.2:g.119929825A=	GRCh38
NC_000023.10:g.119063788A= , CM000685.1:g.119063788A=	GRCh37
NC_000023.9:g.118947816A=	NCBI36
NG_021260.1:g.18948T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371410.5:c.1073+191T= MANE Select	ENSP00000360464.3:n.1073+191T=
ENST00000652253.1:c.1069+191T=
ENST00000371410.4:c.1073+191T=	ENSP00000360464.3:n.1073+191T=
ENST00000477789.5:n.2001+191T=
NM_024528.3:c.1073+191T=	NP_078804.2:n.1073+191T=
XM_017029842.1:c.776+191T=	XP_016885331.1:n.776+191T=
NM_024528.4:c.1073+191T= MANE Select	NP_078804.2:n.1073+191T=