Canonical Allele Identifier: CA414193169
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930034T>C , CM000685.2:g.119930034T>C GRCh38
NC_000023.10:g.119063997T>C , CM000685.1:g.119063997T>C GRCh37
NC_000023.9:g.118948025T>C NCBI36
NG_021260.1:g.18739A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1055A>G MANE Select ENSP00000360464.3:p.Tyr352Cys
ENST00000652253.1:c.1051A>G
ENST00000371410.4:c.1055A>G ENSP00000360464.3:p.Tyr352Cys
ENST00000477789.5:n.1983A>G
NM_024528.3:c.1055A>G NP_078804.2:p.Tyr352Cys
XM_017029842.1:c.758A>G XP_016885331.1:p.Tyr253Cys
NM_024528.4:c.1055A>G MANE Select NP_078804.2:p.Tyr352Cys