Canonical Allele Identifier: CA414193129
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930017T>A , CM000685.2:g.119930017T>A GRCh38
NC_000023.10:g.119063980T>A , CM000685.1:g.119063980T>A GRCh37
NC_000023.9:g.118948008T>A NCBI36
NG_021260.1:g.18756A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1072A>T MANE Select ENSP00000360464.3:p.Arg358Trp
ENST00000652253.1:c.1068A>T
ENST00000371410.4:c.1072A>T ENSP00000360464.3:p.Arg358Trp
ENST00000477789.5:n.2000A>T
NM_024528.3:c.1072A>T NP_078804.2:p.Arg358Trp
XM_017029842.1:c.775A>T XP_016885331.1:p.Arg259Trp
NM_024528.4:c.1072A>T MANE Select NP_078804.2:p.Arg358Trp