Canonical Allele Identifier: CA414193309
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930095G>C , CM000685.2:g.119930095G>C GRCh38
NC_000023.10:g.119064058G>C , CM000685.1:g.119064058G>C GRCh37
NC_000023.9:g.118948086G>C NCBI36
NG_021260.1:g.18678C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.994C>G MANE Select ENSP00000360464.3:p.Pro332Ala
ENST00000652253.1:c.990C>G
ENST00000371410.4:c.994C>G ENSP00000360464.3:p.Pro332Ala
ENST00000477789.5:n.1922C>G
NM_024528.3:c.994C>G NP_078804.2:p.Pro332Ala
XM_017029842.1:c.697C>G XP_016885331.1:p.Pro233Ala
NM_024528.4:c.994C>G MANE Select NP_078804.2:p.Pro332Ala