Canonical Allele Identifier: CA414193279

Gene: NKAP

Linked Data

• MyVariant Identifiers: chrX:g.119064044T>A (hg19) ; chrX:g.119930081T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119930081T>A , CM000685.2:g.119930081T>A	GRCh38
NC_000023.10:g.119064044T>A , CM000685.1:g.119064044T>A	GRCh37
NC_000023.9:g.118948072T>A	NCBI36
NG_021260.1:g.18692A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371410.5:c.1008A>T MANE Select	ENSP00000360464.3:p.Glu336Asp
ENST00000652253.1:c.1004A>T
ENST00000371410.4:c.1008A>T	ENSP00000360464.3:p.Glu336Asp
ENST00000477789.5:n.1936A>T
NM_024528.3:c.1008A>T	NP_078804.2:p.Glu336Asp
XM_017029842.1:c.711A>T	XP_016885331.1:p.Glu237Asp
NM_024528.4:c.1008A>T MANE Select	NP_078804.2:p.Glu336Asp