Canonical Allele Identifier: CA2454711964

Gene: NKAP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119929845T= , CM000685.2:g.119929845T=	GRCh38
NC_000023.10:g.119063808T= , CM000685.1:g.119063808T=	GRCh37
NC_000023.9:g.118947836T=	NCBI36
NG_021260.1:g.18928A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371410.5:c.1073+171A= MANE Select	ENSP00000360464.3:n.1073+171A=
ENST00000652253.1:c.1069+171A=
ENST00000371410.4:c.1073+171A=	ENSP00000360464.3:n.1073+171A=
ENST00000477789.5:n.2001+171A=
NM_024528.3:c.1073+171A=	NP_078804.2:n.1073+171A=
XM_017029842.1:c.776+171A=	XP_016885331.1:n.776+171A=
NM_024528.4:c.1073+171A= MANE Select	NP_078804.2:n.1073+171A=