Canonical Allele Identifier: CA644082778
Gene: NKAP HGNC NCBI

Linked Data

dbSNP Id: rs1473731880
gnomAD v2: X-119064136-G-A
gnomAD v4: X-119930173-G-A
MyVariant Identifiers: chrX:g.119064136G>A (hg19) chrX:g.119930173G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930173G>A , CM000685.2:g.119930173G>A GRCh38
NC_000023.10:g.119064136G>A , CM000685.1:g.119064136G>A GRCh37
NC_000023.9:g.118948164G>A NCBI36
NG_021260.1:g.18600C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.924-8C>T MANE Select ENSP00000360464.3:n.924-8C>T
ENST00000652253.1:c.920-8C>T
ENST00000371410.4:c.924-8C>T ENSP00000360464.3:n.924-8C>T
ENST00000477789.5:n.1852-8C>T
ENST00000482407.1:n.723-8C>T
NM_024528.3:c.924-8C>T NP_078804.2:n.924-8C>T
XM_017029842.1:c.627-8C>T XP_016885331.1:n.627-8C>T
NM_024528.4:c.924-8C>T MANE Select NP_078804.2:n.924-8C>T
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