Canonical Allele Identifier: CA2694579777
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119929988G>A , CM000685.2:g.119929988G>A GRCh38
NC_000023.10:g.119063951G>A , CM000685.1:g.119063951G>A GRCh37
NC_000023.9:g.118947979G>A NCBI36
NG_021260.1:g.18785C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.1073+28C>T MANE Select ENSP00000360464.3:n.1073+28C>T
ENST00000652253.1:c.1069+28C>T
ENST00000371410.4:c.1073+28C>T ENSP00000360464.3:n.1073+28C>T
ENST00000477789.5:n.2001+28C>T
NM_024528.3:c.1073+28C>T NP_078804.2:n.1073+28C>T
XM_017029842.1:c.776+28C>T XP_016885331.1:n.776+28C>T
NM_024528.4:c.1073+28C>T MANE Select NP_078804.2:n.1073+28C>T