Canonical Allele Identifier: CA414193302
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930091C>A , CM000685.2:g.119930091C>A GRCh38
NC_000023.10:g.119064054C>A , CM000685.1:g.119064054C>A GRCh37
NC_000023.9:g.118948082C>A NCBI36
NG_021260.1:g.18682G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.998G>T MANE Select ENSP00000360464.3:p.Arg333Leu
ENST00000652253.1:c.994G>T
ENST00000371410.4:c.998G>T ENSP00000360464.3:p.Arg333Leu
ENST00000477789.5:n.1926G>T
NM_024528.3:c.998G>T NP_078804.2:p.Arg333Leu
XM_017029842.1:c.701G>T XP_016885331.1:p.Arg234Leu
NM_024528.4:c.998G>T MANE Select NP_078804.2:p.Arg333Leu