Canonical Allele Identifier: CA334136027

Gene: NKAP

Linked Data

• dbSNP Id: rs763290218
• gnomAD v3: X-119929942-A-G
• gnomAD v4: X-119929942-A-G
• MyVariant Identifiers: chrX:g.119063905A>G (hg19) ; chrX:g.119929942A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119929942A>G , CM000685.2:g.119929942A>G	GRCh38
NC_000023.10:g.119063905A>G , CM000685.1:g.119063905A>G	GRCh37
NC_000023.9:g.118947933A>G	NCBI36
NG_021260.1:g.18831T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371410.5:c.1073+74T>C MANE Select	ENSP00000360464.3:n.1073+74T>C
ENST00000652253.1:c.1069+74T>C
ENST00000371410.4:c.1073+74T>C	ENSP00000360464.3:n.1073+74T>C
ENST00000477789.5:n.2001+74T>C
NM_024528.3:c.1073+74T>C	NP_078804.2:n.1073+74T>C
XM_017029842.1:c.776+74T>C	XP_016885331.1:n.776+74T>C
NM_024528.4:c.1073+74T>C MANE Select	NP_078804.2:n.1073+74T>C