Canonical Allele Identifier: CA334135986
Gene: NKAP HGNC NCBI

Linked Data

dbSNP Id: rs746387418
MyVariant Identifiers: chrX:g.119063824T>G (hg19) chrX:g.119929861T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119929861T>G , CM000685.2:g.119929861T>G GRCh38
NC_000023.10:g.119063824T>G , CM000685.1:g.119063824T>G GRCh37
NC_000023.9:g.118947852T>G NCBI36
NG_021260.1:g.18912A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.1073+155A>C MANE Select ENSP00000360464.3:n.1073+155A>C
ENST00000652253.1:c.1069+155A>C
ENST00000371410.4:c.1073+155A>C ENSP00000360464.3:n.1073+155A>C
ENST00000477789.5:n.2001+155A>C
NM_024528.3:c.1073+155A>C NP_078804.2:n.1073+155A>C
XM_017029842.1:c.776+155A>C XP_016885331.1:n.776+155A>C
NM_024528.4:c.1073+155A>C MANE Select NP_078804.2:n.1073+155A>C
Search 100 bp 5'
Search 100 bp 3'