Canonical Allele Identifier: CA2694579749
Gene: NKAP HGNC NCBI

Linked Data

gnomAD v4: X-119929941-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119929941C>T , CM000685.2:g.119929941C>T GRCh38
NC_000023.10:g.119063904C>T , CM000685.1:g.119063904C>T GRCh37
NC_000023.9:g.118947932C>T NCBI36
NG_021260.1:g.18832G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.1073+75G>A MANE Select ENSP00000360464.3:n.1073+75G>A
ENST00000652253.1:c.1069+75G>A
ENST00000371410.4:c.1073+75G>A ENSP00000360464.3:n.1073+75G>A
ENST00000477789.5:n.2001+75G>A
NM_024528.3:c.1073+75G>A NP_078804.2:n.1073+75G>A
XM_017029842.1:c.776+75G>A XP_016885331.1:n.776+75G>A
NM_024528.4:c.1073+75G>A MANE Select NP_078804.2:n.1073+75G>A
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