Canonical Allele Identifier: CA414193390
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.959C>G MANE Select ENSP00000360464.3:p.Ala320Gly
ENST00000652253.1:c.955C>G
ENST00000371410.4:c.959C>G ENSP00000360464.3:p.Ala320Gly
ENST00000477789.5:n.1887C>G
ENST00000482407.1:n.758C>G
NM_024528.3:c.959C>G NP_078804.2:p.Ala320Gly
XM_017029842.1:c.662C>G XP_016885331.1:p.Ala221Gly
NM_024528.4:c.959C>G MANE Select NP_078804.2:p.Ala320Gly