Canonical Allele Identifier: CA414193426
Gene: NKAP HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.119064109G>C (hg19) chrX:g.119930146G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930146G>C , CM000685.2:g.119930146G>C GRCh38
NC_000023.10:g.119064109G>C , CM000685.1:g.119064109G>C GRCh37
NC_000023.9:g.118948137G>C NCBI36
NG_021260.1:g.18627C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.943C>G MANE Select ENSP00000360464.3:p.Pro315Ala
ENST00000652253.1:c.939C>G
ENST00000371410.4:c.943C>G ENSP00000360464.3:p.Pro315Ala
ENST00000477789.5:n.1871C>G
ENST00000482407.1:n.742C>G
NM_024528.3:c.943C>G NP_078804.2:p.Pro315Ala
XM_017029842.1:c.646C>G XP_016885331.1:p.Pro216Ala
NM_024528.4:c.943C>G MANE Select NP_078804.2:p.Pro315Ala
Search 100 bp 5'
Search 100 bp 3'