Canonical Allele Identifier: CA414193179
Gene: NKAP HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.119064001C>T (hg19) chrX:g.119930038C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930038C>T , CM000685.2:g.119930038C>T GRCh38
NC_000023.10:g.119064001C>T , CM000685.1:g.119064001C>T GRCh37
NC_000023.9:g.118948029C>T NCBI36
NG_021260.1:g.18735G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1051G>A MANE Select ENSP00000360464.3:p.Gly351Ser
ENST00000652253.1:c.1047G>A
ENST00000371410.4:c.1051G>A ENSP00000360464.3:p.Gly351Ser
ENST00000477789.5:n.1979G>A
NM_024528.3:c.1051G>A NP_078804.2:p.Gly351Ser
XM_017029842.1:c.754G>A XP_016885331.1:p.Gly252Ser
NM_024528.4:c.1051G>A MANE Select NP_078804.2:p.Gly351Ser
Search 100 bp 5'
Search 100 bp 3'