Canonical Allele Identifier: CA414193471
Gene: NKAP HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.119064129C>T (hg19) chrX:g.119930166C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930166C>T , CM000685.2:g.119930166C>T GRCh38
NC_000023.10:g.119064129C>T , CM000685.1:g.119064129C>T GRCh37
NC_000023.9:g.118948157C>T NCBI36
NG_021260.1:g.18607G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.924-1G>A MANE Select ENSP00000360464.3:n.924-1G>A
ENST00000652253.1:c.920-1G>A
ENST00000371410.4:c.924-1G>A ENSP00000360464.3:n.924-1G>A
ENST00000477789.5:n.1852-1G>A
ENST00000482407.1:n.723-1G>A
NM_024528.3:c.924-1G>A NP_078804.2:n.924-1G>A
XM_017029842.1:c.627-1G>A XP_016885331.1:n.627-1G>A
NM_024528.4:c.924-1G>A MANE Select NP_078804.2:n.924-1G>A
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