Canonical Allele Identifier: CA414193162
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930031A>T , CM000685.2:g.119930031A>T GRCh38
NC_000023.10:g.119063994A>T , CM000685.1:g.119063994A>T GRCh37
NC_000023.9:g.118948022A>T NCBI36
NG_021260.1:g.18742T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1058T>A MANE Select ENSP00000360464.3:p.Val353Glu
ENST00000652253.1:c.1054T>A
ENST00000371410.4:c.1058T>A ENSP00000360464.3:p.Val353Glu
ENST00000477789.5:n.1986T>A
NM_024528.3:c.1058T>A NP_078804.2:p.Val353Glu
XM_017029842.1:c.761T>A XP_016885331.1:p.Val254Glu
NM_024528.4:c.1058T>A MANE Select NP_078804.2:p.Val353Glu