Canonical Allele Identifier: CA414193219
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930056C>A , CM000685.2:g.119930056C>A GRCh38
NC_000023.10:g.119064019C>A , CM000685.1:g.119064019C>A GRCh37
NC_000023.9:g.118948047C>A NCBI36
NG_021260.1:g.18717G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.1033G>T MANE Select ENSP00000360464.3:p.Ala345Ser
ENST00000652253.1:c.1029G>T
ENST00000371410.4:c.1033G>T ENSP00000360464.3:p.Ala345Ser
ENST00000477789.5:n.1961G>T
NM_024528.3:c.1033G>T NP_078804.2:p.Ala345Ser
XM_017029842.1:c.736G>T XP_016885331.1:p.Ala246Ser
NM_024528.4:c.1033G>T MANE Select NP_078804.2:p.Ala345Ser