Canonical Allele Identifier: CA518222043

Gene: NKAP

Linked Data

• MyVariant Identifiers: chrX:g.119064035C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119930072C>T , CM000685.2:g.119930072C>T	GRCh38
NC_000023.10:g.119064035C>T , CM000685.1:g.119064035C>T	GRCh37
NC_000023.9:g.118948063C>T	NCBI36
NG_021260.1:g.18701G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371410.5:c.1017G>A MANE Select	ENSP00000360464.3:p.Leu339=
ENST00000652253.1:c.1013G>A
ENST00000371410.4:c.1017G>A	ENSP00000360464.3:p.Leu339=
ENST00000477789.5:n.1945G>A
NM_024528.3:c.1017G>A	NP_078804.2:p.Leu339=
XM_017029842.1:c.720G>A	XP_016885331.1:p.Leu240=
NM_024528.4:c.1017G>A MANE Select	NP_078804.2:p.Leu339=