Canonical Allele Identifier: CA2454711970
Gene: NKAP HGNC NCBI

Linked Data

dbSNP Id: rs1603379760
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119929877A>G , CM000685.2:g.119929877A>G GRCh38
NC_000023.10:g.119063840A>G , CM000685.1:g.119063840A>G GRCh37
NC_000023.9:g.118947868A>G NCBI36
NG_021260.1:g.18896T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1073+139T>C MANE Select ENSP00000360464.3:n.1073+139T>C
ENST00000652253.1:c.1069+139T>C
ENST00000371410.4:c.1073+139T>C ENSP00000360464.3:n.1073+139T>C
ENST00000477789.5:n.2001+139T>C
NM_024528.3:c.1073+139T>C NP_078804.2:n.1073+139T>C
XM_017029842.1:c.776+139T>C XP_016885331.1:n.776+139T>C
NM_024528.4:c.1073+139T>C MANE Select NP_078804.2:n.1073+139T>C
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