Canonical Allele Identifier: CA414193133
Gene: NKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930019C>G , CM000685.2:g.119930019C>G GRCh38
NC_000023.10:g.119063982C>G , CM000685.1:g.119063982C>G GRCh37
NC_000023.9:g.118948010C>G NCBI36
NG_021260.1:g.18754G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1070G>C MANE Select ENSP00000360464.3:p.Ser357Thr
ENST00000652253.1:c.1066G>C
ENST00000371410.4:c.1070G>C ENSP00000360464.3:p.Ser357Thr
ENST00000477789.5:n.1998G>C
NM_024528.3:c.1070G>C NP_078804.2:p.Ser357Thr
XM_017029842.1:c.773G>C XP_016885331.1:p.Ser258Thr
NM_024528.4:c.1070G>C MANE Select NP_078804.2:p.Ser357Thr