Canonical Allele Identifier: CA518222085
Gene: NKAP HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.119064095T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930132T>A , CM000685.2:g.119930132T>A GRCh38
NC_000023.10:g.119064095T>A , CM000685.1:g.119064095T>A GRCh37
NC_000023.9:g.118948123T>A NCBI36
NG_021260.1:g.18641A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.957A>T MANE Select ENSP00000360464.3:p.Ala319=
ENST00000652253.1:c.953A>T
ENST00000371410.4:c.957A>T ENSP00000360464.3:p.Ala319=
ENST00000477789.5:n.1885A>T
ENST00000482407.1:n.756A>T
NM_024528.3:c.957A>T NP_078804.2:p.Ala319=
XM_017029842.1:c.660A>T XP_016885331.1:p.Ala220=
NM_024528.4:c.957A>T MANE Select NP_078804.2:p.Ala319=
Search 100 bp 5'
Search 100 bp 3'