Canonical Allele Identifier: CA414193313
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930097A>G , CM000685.2:g.119930097A>G GRCh38
NC_000023.10:g.119064060A>G , CM000685.1:g.119064060A>G GRCh37
NC_000023.9:g.118948088A>G NCBI36
NG_021260.1:g.18676T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.992T>C MANE Select ENSP00000360464.3:p.Ile331Thr
ENST00000652253.1:c.988T>C
ENST00000371410.4:c.992T>C ENSP00000360464.3:p.Ile331Thr
ENST00000477789.5:n.1920T>C
NM_024528.3:c.992T>C NP_078804.2:p.Ile331Thr
XM_017029842.1:c.695T>C XP_016885331.1:p.Ile232Thr
NM_024528.4:c.992T>C MANE Select NP_078804.2:p.Ile331Thr