Canonical Allele Identifier: CA414193389
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930130G>A , CM000685.2:g.119930130G>A GRCh38
NC_000023.10:g.119064093G>A , CM000685.1:g.119064093G>A GRCh37
NC_000023.9:g.118948121G>A NCBI36
NG_021260.1:g.18643C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.959C>T MANE Select ENSP00000360464.3:p.Ala320Val
ENST00000652253.1:c.955C>T
ENST00000371410.4:c.959C>T ENSP00000360464.3:p.Ala320Val
ENST00000477789.5:n.1887C>T
ENST00000482407.1:n.758C>T
NM_024528.3:c.959C>T NP_078804.2:p.Ala320Val
XM_017029842.1:c.662C>T XP_016885331.1:p.Ala221Val
NM_024528.4:c.959C>T MANE Select NP_078804.2:p.Ala320Val