Canonical Allele Identifier: CA518222058
Gene: NKAP HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.119064056T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930093T>A , CM000685.2:g.119930093T>A GRCh38
NC_000023.10:g.119064056T>A , CM000685.1:g.119064056T>A GRCh37
NC_000023.9:g.118948084T>A NCBI36
NG_021260.1:g.18680A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.996A>T MANE Select ENSP00000360464.3:p.Pro332=
ENST00000652253.1:c.992A>T
ENST00000371410.4:c.996A>T ENSP00000360464.3:p.Pro332=
ENST00000477789.5:n.1924A>T
NM_024528.3:c.996A>T NP_078804.2:p.Pro332=
XM_017029842.1:c.699A>T XP_016885331.1:p.Pro233=
NM_024528.4:c.996A>T MANE Select NP_078804.2:p.Pro332=