Canonical Allele Identifier: CA414193370
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930121T>G , CM000685.2:g.119930121T>G GRCh38
NC_000023.10:g.119064084T>G , CM000685.1:g.119064084T>G GRCh37
NC_000023.9:g.118948112T>G NCBI36
NG_021260.1:g.18652A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.968A>C MANE Select ENSP00000360464.3:p.Glu323Ala
ENST00000652253.1:c.964A>C
ENST00000371410.4:c.968A>C ENSP00000360464.3:p.Glu323Ala
ENST00000477789.5:n.1896A>C
NM_024528.3:c.968A>C NP_078804.2:p.Glu323Ala
XM_017029842.1:c.671A>C XP_016885331.1:p.Glu224Ala
NM_024528.4:c.968A>C MANE Select NP_078804.2:p.Glu323Ala