Canonical Allele Identifier: CA644082775

Gene: NKAP

Linked Data

• dbSNP Id: rs1487548970
• gnomAD v2: X-119063793-CATAT-C
• gnomAD v3: X-119929830-CATAT-C
• gnomAD v4: X-119929830-CATAT-C
• MyVariant Identifiers: chrX:g.119063794_119063797del (hg19) ; chrX:g.119929831_119929834del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119929834_119929837del , CM000685.2:g.119929834_119929837del	GRCh38
NC_000023.10:g.119063797_119063800del , CM000685.1:g.119063797_119063800del	GRCh37
NC_000023.9:g.118947825_118947828del	NCBI36
NG_021260.1:g.18939_18942del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371410.5:c.1073+182_1073+185del MANE Select	ENSP00000360464.3:n.1073+182_1073+185del
ENST00000652253.1:c.1069+182_1069+185del
ENST00000371410.4:c.1073+182_1073+185del	ENSP00000360464.3:n.1073+182_1073+185del
ENST00000477789.5:n.2001+182_2001+185del
NM_024528.3:c.1073+182_1073+185del	NP_078804.2:n.1073+182_1073+185del
XM_017029842.1:c.776+182_776+185del	XP_016885331.1:n.776+182_776+185del
NM_024528.4:c.1073+182_1073+185del MANE Select	NP_078804.2:n.1073+182_1073+185del