Canonical Allele Identifier: CA518222026
Gene: NKAP HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.119064002T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930039T>G , CM000685.2:g.119930039T>G GRCh38
NC_000023.10:g.119064002T>G , CM000685.1:g.119064002T>G GRCh37
NC_000023.9:g.118948030T>G NCBI36
NG_021260.1:g.18734A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1050A>C MANE Select ENSP00000360464.3:p.Ser350=
ENST00000652253.1:c.1046A>C
ENST00000371410.4:c.1050A>C ENSP00000360464.3:p.Ser350=
ENST00000477789.5:n.1978A>C
NM_024528.3:c.1050A>C NP_078804.2:p.Ser350=
XM_017029842.1:c.753A>C XP_016885331.1:p.Ser251=
NM_024528.4:c.1050A>C MANE Select NP_078804.2:p.Ser350=
Search 100 bp 5'
Search 100 bp 3'