Canonical Allele Identifier: CA414193340
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930109G>T , CM000685.2:g.119930109G>T GRCh38
NC_000023.10:g.119064072G>T , CM000685.1:g.119064072G>T GRCh37
NC_000023.9:g.118948100G>T NCBI36
NG_021260.1:g.18664C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.980C>A MANE Select ENSP00000360464.3:p.Ala327Asp
ENST00000652253.1:c.976C>A
ENST00000371410.4:c.980C>A ENSP00000360464.3:p.Ala327Asp
ENST00000477789.5:n.1908C>A
NM_024528.3:c.980C>A NP_078804.2:p.Ala327Asp
XM_017029842.1:c.683C>A XP_016885331.1:p.Ala228Asp
NM_024528.4:c.980C>A MANE Select NP_078804.2:p.Ala327Asp