Canonical Allele Identifier: CA518222051
Gene: NKAP HGNC NCBI

Linked Data

dbSNP Id: rs1603379774
MyVariant Identifiers: chrX:g.119064047A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930084A>C , CM000685.2:g.119930084A>C GRCh38
NC_000023.10:g.119064047A>C , CM000685.1:g.119064047A>C GRCh37
NC_000023.9:g.118948075A>C NCBI36
NG_021260.1:g.18689T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.1005T>G MANE Select ENSP00000360464.3:p.Gly335=
ENST00000652253.1:c.1001T>G
ENST00000371410.4:c.1005T>G ENSP00000360464.3:p.Gly335=
ENST00000477789.5:n.1933T>G
NM_024528.3:c.1005T>G NP_078804.2:p.Gly335=
XM_017029842.1:c.708T>G XP_016885331.1:p.Gly236=
NM_024528.4:c.1005T>G MANE Select NP_078804.2:p.Gly335=