Canonical Allele Identifier: CA2694579771
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119929980T>C , CM000685.2:g.119929980T>C GRCh38
NC_000023.10:g.119063943T>C , CM000685.1:g.119063943T>C GRCh37
NC_000023.9:g.118947971T>C NCBI36
NG_021260.1:g.18793A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.1073+36A>G MANE Select ENSP00000360464.3:n.1073+36A>G
ENST00000652253.1:c.1069+36A>G
ENST00000371410.4:c.1073+36A>G ENSP00000360464.3:n.1073+36A>G
ENST00000477789.5:n.2001+36A>G
NM_024528.3:c.1073+36A>G NP_078804.2:n.1073+36A>G
XM_017029842.1:c.776+36A>G XP_016885331.1:n.776+36A>G
NM_024528.4:c.1073+36A>G MANE Select NP_078804.2:n.1073+36A>G