Canonical Allele Identifier: CA518222032
Gene: NKAP HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.119064017T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930054T>G , CM000685.2:g.119930054T>G GRCh38
NC_000023.10:g.119064017T>G , CM000685.1:g.119064017T>G GRCh37
NC_000023.9:g.118948045T>G NCBI36
NG_021260.1:g.18719A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.1035A>C MANE Select ENSP00000360464.3:p.Ala345=
ENST00000652253.1:c.1031A>C
ENST00000371410.4:c.1035A>C ENSP00000360464.3:p.Ala345=
ENST00000477789.5:n.1963A>C
NM_024528.3:c.1035A>C NP_078804.2:p.Ala345=
XM_017029842.1:c.738A>C XP_016885331.1:p.Ala246=
NM_024528.4:c.1035A>C MANE Select NP_078804.2:p.Ala345=