Canonical Allele Identifier: CA518222027
Gene: NKAP HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.119064008T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930045T>C , CM000685.2:g.119930045T>C GRCh38
NC_000023.10:g.119064008T>C , CM000685.1:g.119064008T>C GRCh37
NC_000023.9:g.118948036T>C NCBI36
NG_021260.1:g.18728A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.1044A>G MANE Select ENSP00000360464.3:p.Glu348=
ENST00000652253.1:c.1040A>G
ENST00000371410.4:c.1044A>G ENSP00000360464.3:p.Glu348=
ENST00000477789.5:n.1972A>G
NM_024528.3:c.1044A>G NP_078804.2:p.Glu348=
XM_017029842.1:c.747A>G XP_016885331.1:p.Glu249=
NM_024528.4:c.1044A>G MANE Select NP_078804.2:p.Glu348=
Search 100 bp 5'
Search 100 bp 3'