Canonical Allele Identifier: CA414193182
Gene: NKAP HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.119064003G>T (hg19) chrX:g.119930040G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930040G>T , CM000685.2:g.119930040G>T GRCh38
NC_000023.10:g.119064003G>T , CM000685.1:g.119064003G>T GRCh37
NC_000023.9:g.118948031G>T NCBI36
NG_021260.1:g.18733C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1049C>A MANE Select ENSP00000360464.3:p.Ser350Ter
ENST00000652253.1:c.1045C>A
ENST00000371410.4:c.1049C>A ENSP00000360464.3:p.Ser350Ter
ENST00000477789.5:n.1977C>A
NM_024528.3:c.1049C>A NP_078804.2:p.Ser350Ter
XM_017029842.1:c.752C>A XP_016885331.1:p.Ser251Ter
NM_024528.4:c.1049C>A MANE Select NP_078804.2:p.Ser350Ter
Search 100 bp 5'
Search 100 bp 3'