Canonical Allele Identifier: CA414193364
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930119A>T , CM000685.2:g.119930119A>T GRCh38
NC_000023.10:g.119064082A>T , CM000685.1:g.119064082A>T GRCh37
NC_000023.9:g.118948110A>T NCBI36
NG_021260.1:g.18654T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.970T>A MANE Select ENSP00000360464.3:p.Tyr324Asn
ENST00000652253.1:c.966T>A
ENST00000371410.4:c.970T>A ENSP00000360464.3:p.Tyr324Asn
ENST00000477789.5:n.1898T>A
NM_024528.3:c.970T>A NP_078804.2:p.Tyr324Asn
XM_017029842.1:c.673T>A XP_016885331.1:p.Tyr225Asn
NM_024528.4:c.970T>A MANE Select NP_078804.2:p.Tyr324Asn