Canonical Allele Identifier: CA414193127
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930016C>T , CM000685.2:g.119930016C>T GRCh38
NC_000023.10:g.119063979C>T , CM000685.1:g.119063979C>T GRCh37
NC_000023.9:g.118948007C>T NCBI36
NG_021260.1:g.18757G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1073G>A MANE Select ENSP00000360464.3:p.Arg358Lys
ENST00000652253.1:c.1069G>A
ENST00000371410.4:c.1073G>A ENSP00000360464.3:p.Arg358Lys
ENST00000477789.5:n.2001G>A
NM_024528.3:c.1073G>A NP_078804.2:p.Arg358Lys
XM_017029842.1:c.776G>A XP_016885331.1:p.Arg259Lys
NM_024528.4:c.1073G>A MANE Select NP_078804.2:p.Arg358Lys