Canonical Allele Identifier: CA414193160
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930029T>C , CM000685.2:g.119930029T>C GRCh38
NC_000023.10:g.119063992T>C , CM000685.1:g.119063992T>C GRCh37
NC_000023.9:g.118948020T>C NCBI36
NG_021260.1:g.18744A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1060A>G MANE Select ENSP00000360464.3:p.Met354Val
ENST00000652253.1:c.1056A>G
ENST00000371410.4:c.1060A>G ENSP00000360464.3:p.Met354Val
ENST00000477789.5:n.1988A>G
NM_024528.3:c.1060A>G NP_078804.2:p.Met354Val
XM_017029842.1:c.763A>G XP_016885331.1:p.Met255Val
NM_024528.4:c.1060A>G MANE Select NP_078804.2:p.Met354Val