Canonical Allele Identifier: CA518222056

Gene: NKAP

Linked Data

• MyVariant Identifiers: chrX:g.119064053T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119930090T>G , CM000685.2:g.119930090T>G	GRCh38
NC_000023.10:g.119064053T>G , CM000685.1:g.119064053T>G	GRCh37
NC_000023.9:g.118948081T>G	NCBI36
NG_021260.1:g.18683A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371410.5:c.999A>C MANE Select	ENSP00000360464.3:p.Arg333=
ENST00000652253.1:c.995A>C
ENST00000371410.4:c.999A>C	ENSP00000360464.3:p.Arg333=
ENST00000477789.5:n.1927A>C
NM_024528.3:c.999A>C	NP_078804.2:p.Arg333=
XM_017029842.1:c.702A>C	XP_016885331.1:p.Arg234=
NM_024528.4:c.999A>C MANE Select	NP_078804.2:p.Arg333=