Canonical Allele Identifier: CA870719216
Gene: NKAP HGNC NCBI

Linked Data

dbSNP Id: rs1271494335
gnomAD v3: X-119929833-A-G
gnomAD v4: X-119929833-A-G
MyVariant Identifiers: chrX:g.119063796A>G (hg19) chrX:g.119929833A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119929833A>G , CM000685.2:g.119929833A>G GRCh38
NC_000023.10:g.119063796A>G , CM000685.1:g.119063796A>G GRCh37
NC_000023.9:g.118947824A>G NCBI36
NG_021260.1:g.18940T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.1073+183T>C MANE Select ENSP00000360464.3:n.1073+183T>C
ENST00000652253.1:c.1069+183T>C
ENST00000371410.4:c.1073+183T>C ENSP00000360464.3:n.1073+183T>C
ENST00000477789.5:n.2001+183T>C
NM_024528.3:c.1073+183T>C NP_078804.2:n.1073+183T>C
XM_017029842.1:c.776+183T>C XP_016885331.1:n.776+183T>C
NM_024528.4:c.1073+183T>C MANE Select NP_078804.2:n.1073+183T>C
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