Canonical Allele Identifier: CA414193261
Gene: NKAP HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.119064036A>C (hg19) chrX:g.119930073A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930073A>C , CM000685.2:g.119930073A>C GRCh38
NC_000023.10:g.119064036A>C , CM000685.1:g.119064036A>C GRCh37
NC_000023.9:g.118948064A>C NCBI36
NG_021260.1:g.18700T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.1016T>G MANE Select ENSP00000360464.3:p.Leu339Trp
ENST00000652253.1:c.1012T>G
ENST00000371410.4:c.1016T>G ENSP00000360464.3:p.Leu339Trp
ENST00000477789.5:n.1944T>G
NM_024528.3:c.1016T>G NP_078804.2:p.Leu339Trp
XM_017029842.1:c.719T>G XP_016885331.1:p.Leu240Trp
NM_024528.4:c.1016T>G MANE Select NP_078804.2:p.Leu339Trp
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