Canonical Allele Identifier: CA518222059
Gene: NKAP HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.119064056T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930093T>C , CM000685.2:g.119930093T>C GRCh38
NC_000023.10:g.119064056T>C , CM000685.1:g.119064056T>C GRCh37
NC_000023.9:g.118948084T>C NCBI36
NG_021260.1:g.18680A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.996A>G MANE Select ENSP00000360464.3:p.Pro332=
ENST00000652253.1:c.992A>G
ENST00000371410.4:c.996A>G ENSP00000360464.3:p.Pro332=
ENST00000477789.5:n.1924A>G
NM_024528.3:c.996A>G NP_078804.2:p.Pro332=
XM_017029842.1:c.699A>G XP_016885331.1:p.Pro233=
NM_024528.4:c.996A>G MANE Select NP_078804.2:p.Pro332=