Canonical Allele Identifier: CA414193393
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930131C>G , CM000685.2:g.119930131C>G GRCh38
NC_000023.10:g.119064094C>G , CM000685.1:g.119064094C>G GRCh37
NC_000023.9:g.118948122C>G NCBI36
NG_021260.1:g.18642G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.958G>C MANE Select ENSP00000360464.3:p.Ala320Pro
ENST00000652253.1:c.954G>C
ENST00000371410.4:c.958G>C ENSP00000360464.3:p.Ala320Pro
ENST00000477789.5:n.1886G>C
ENST00000482407.1:n.757G>C
NM_024528.3:c.958G>C NP_078804.2:p.Ala320Pro
XM_017029842.1:c.661G>C XP_016885331.1:p.Ala221Pro
NM_024528.4:c.958G>C MANE Select NP_078804.2:p.Ala320Pro