Canonical Allele Identifier: CA2454712025
Gene: NKAP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930194G= , CM000685.2:g.119930194G= GRCh38
NC_000023.10:g.119064157G= , CM000685.1:g.119064157G= GRCh37
NC_000023.9:g.118948185G= NCBI36
NG_021260.1:g.18579C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.924-29C= MANE Select ENSP00000360464.3:n.924-29C=
ENST00000652253.1:c.920-29C=
ENST00000371410.4:c.924-29C= ENSP00000360464.3:n.924-29C=
ENST00000477789.5:n.1852-29C=
ENST00000482407.1:n.723-29C=
NM_024528.3:c.924-29C= NP_078804.2:n.924-29C=
XM_017029842.1:c.627-29C= XP_016885331.1:n.627-29C=
NM_024528.4:c.924-29C= MANE Select NP_078804.2:n.924-29C=
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