Canonical Allele Identifier: CA414193157
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930028A>T , CM000685.2:g.119930028A>T GRCh38
NC_000023.10:g.119063991A>T , CM000685.1:g.119063991A>T GRCh37
NC_000023.9:g.118948019A>T NCBI36
NG_021260.1:g.18745T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1061T>A MANE Select ENSP00000360464.3:p.Met354Lys
ENST00000652253.1:c.1057T>A
ENST00000371410.4:c.1061T>A ENSP00000360464.3:p.Met354Lys
ENST00000477789.5:n.1989T>A
NM_024528.3:c.1061T>A NP_078804.2:p.Met354Lys
XM_017029842.1:c.764T>A XP_016885331.1:p.Met255Lys
NM_024528.4:c.1061T>A MANE Select NP_078804.2:p.Met354Lys