Canonical Allele Identifier: CA414193365
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930119A>C , CM000685.2:g.119930119A>C GRCh38
NC_000023.10:g.119064082A>C , CM000685.1:g.119064082A>C GRCh37
NC_000023.9:g.118948110A>C NCBI36
NG_021260.1:g.18654T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.970T>G MANE Select ENSP00000360464.3:p.Tyr324Asp
ENST00000652253.1:c.966T>G
ENST00000371410.4:c.970T>G ENSP00000360464.3:p.Tyr324Asp
ENST00000477789.5:n.1898T>G
NM_024528.3:c.970T>G NP_078804.2:p.Tyr324Asp
XM_017029842.1:c.673T>G XP_016885331.1:p.Tyr225Asp
NM_024528.4:c.970T>G MANE Select NP_078804.2:p.Tyr324Asp