Canonical Allele Identifier: CA10503715

Gene: NKAP

Linked Data

• dbSNP Id: rs769991780
• ExAC: X:119063966 G / A
• gnomAD v2: X-119063966-G-A
• gnomAD v3: X-119930003-G-A
• gnomAD v4: X-119930003-G-A
• MyVariant Identifiers: chrX:g.119063966G>A (hg19) ; chrX:g.119930003G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119930003G>A , CM000685.2:g.119930003G>A	GRCh38
NC_000023.10:g.119063966G>A , CM000685.1:g.119063966G>A	GRCh37
NC_000023.9:g.118947994G>A	NCBI36
NG_021260.1:g.18770C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371410.5:c.1073+13C>T MANE Select	ENSP00000360464.3:n.1073+13C>T
ENST00000652253.1:c.1069+13C>T
ENST00000371410.4:c.1073+13C>T	ENSP00000360464.3:n.1073+13C>T
ENST00000477789.5:n.2001+13C>T
NM_024528.3:c.1073+13C>T	NP_078804.2:n.1073+13C>T
XM_017029842.1:c.776+13C>T	XP_016885331.1:n.776+13C>T
NM_024528.4:c.1073+13C>T MANE Select	NP_078804.2:n.1073+13C>T