Canonical Allele Identifier: CA414193461

Gene: NKAP

Linked Data

• MyVariant Identifiers: chrX:g.119064126T>G (hg19) ; chrX:g.119930163T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119930163T>G , CM000685.2:g.119930163T>G	GRCh38
NC_000023.10:g.119064126T>G , CM000685.1:g.119064126T>G	GRCh37
NC_000023.9:g.118948154T>G	NCBI36
NG_021260.1:g.18610A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371410.5:c.926A>C MANE Select	ENSP00000360464.3:p.Tyr309Ser
ENST00000652253.1:c.922A>C
ENST00000371410.4:c.926A>C	ENSP00000360464.3:p.Tyr309Ser
ENST00000477789.5:n.1854A>C
ENST00000482407.1:n.725A>C
NM_024528.3:c.926A>C	NP_078804.2:p.Tyr309Ser
XM_017029842.1:c.629A>C	XP_016885331.1:p.Tyr210Ser
NM_024528.4:c.926A>C MANE Select	NP_078804.2:p.Tyr309Ser