Canonical Allele Identifier: CA10503729

Gene: NKAP

Linked Data

• dbSNP Id: rs370283339
• ExAC: X:119064164 A / G
• gnomAD v2: X-119064164-A-G
• gnomAD v3: X-119930201-A-G
• gnomAD v4: X-119930201-A-G
• COSMIC: COSN19708744
• MyVariant Identifiers: chrX:g.119064164A>G (hg19) ; chrX:g.119930201A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119930201A>G , CM000685.2:g.119930201A>G	GRCh38
NC_000023.10:g.119064164A>G , CM000685.1:g.119064164A>G	GRCh37
NC_000023.9:g.118948192A>G	NCBI36
NG_021260.1:g.18572T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371410.5:c.924-36T>C MANE Select	ENSP00000360464.3:n.924-36T>C
ENST00000652253.1:c.920-36T>C
ENST00000371410.4:c.924-36T>C	ENSP00000360464.3:n.924-36T>C
ENST00000477789.5:n.1852-36T>C
ENST00000482407.1:n.723-36T>C
NM_024528.3:c.924-36T>C	NP_078804.2:n.924-36T>C
XM_017029842.1:c.627-36T>C	XP_016885331.1:n.627-36T>C
NM_024528.4:c.924-36T>C MANE Select	NP_078804.2:n.924-36T>C