Canonical Allele Identifier: CA414193374
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930124G>A , CM000685.2:g.119930124G>A GRCh38
NC_000023.10:g.119064087G>A , CM000685.1:g.119064087G>A GRCh37
NC_000023.9:g.118948115G>A NCBI36
NG_021260.1:g.18649C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.965C>T MANE Select ENSP00000360464.3:p.Ala322Val
ENST00000652253.1:c.961C>T
ENST00000371410.4:c.965C>T ENSP00000360464.3:p.Ala322Val
ENST00000477789.5:n.1893C>T
NM_024528.3:c.965C>T NP_078804.2:p.Ala322Val
XM_017029842.1:c.668C>T XP_016885331.1:p.Ala223Val
NM_024528.4:c.965C>T MANE Select NP_078804.2:p.Ala322Val