Canonical Allele Identifier: CA2549834835
Gene: NKAP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119929980T>A , CM000685.2:g.119929980T>A GRCh38
NC_000023.10:g.119063943T>A , CM000685.1:g.119063943T>A GRCh37
NC_000023.9:g.118947971T>A NCBI36
NG_021260.1:g.18793A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1073+36A>T MANE Select ENSP00000360464.3:n.1073+36A>T
ENST00000652253.1:c.1069+36A>T
ENST00000371410.4:c.1073+36A>T ENSP00000360464.3:n.1073+36A>T
ENST00000477789.5:n.2001+36A>T
NM_024528.3:c.1073+36A>T NP_078804.2:n.1073+36A>T
XM_017029842.1:c.776+36A>T XP_016885331.1:n.776+36A>T
NM_024528.4:c.1073+36A>T MANE Select NP_078804.2:n.1073+36A>T
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