Canonical Allele Identifier: CA644082774
Gene: NKAP HGNC NCBI

Linked Data

dbSNP Id: rs1357771960
gnomAD v2: X-119063788-A-C
gnomAD v3: X-119929825-A-C
gnomAD v4: X-119929825-A-C
MyVariant Identifiers: chrX:g.119063788A>C (hg19) chrX:g.119929825A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119929825A>C , CM000685.2:g.119929825A>C GRCh38
NC_000023.10:g.119063788A>C , CM000685.1:g.119063788A>C GRCh37
NC_000023.9:g.118947816A>C NCBI36
NG_021260.1:g.18948T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1073+191T>G MANE Select ENSP00000360464.3:n.1073+191T>G
ENST00000652253.1:c.1069+191T>G
ENST00000371410.4:c.1073+191T>G ENSP00000360464.3:n.1073+191T>G
ENST00000477789.5:n.2001+191T>G
NM_024528.3:c.1073+191T>G NP_078804.2:n.1073+191T>G
XM_017029842.1:c.776+191T>G XP_016885331.1:n.776+191T>G
NM_024528.4:c.1073+191T>G MANE Select NP_078804.2:n.1073+191T>G
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