Canonical Allele Identifier: CA518222075
Gene: NKAP HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.119064077T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930114T>C , CM000685.2:g.119930114T>C GRCh38
NC_000023.10:g.119064077T>C , CM000685.1:g.119064077T>C GRCh37
NC_000023.9:g.118948105T>C NCBI36
NG_021260.1:g.18659A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.975A>G MANE Select ENSP00000360464.3:p.Val325=
ENST00000652253.1:c.971A>G
ENST00000371410.4:c.975A>G ENSP00000360464.3:p.Val325=
ENST00000477789.5:n.1903A>G
NM_024528.3:c.975A>G NP_078804.2:p.Val325=
XM_017029842.1:c.678A>G XP_016885331.1:p.Val226=
NM_024528.4:c.975A>G MANE Select NP_078804.2:p.Val325=