Canonical Allele Identifier: CA2454711960
Gene: NKAP HGNC NCBI

Linked Data

dbSNP Id: rs2056732240
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119929841G>C , CM000685.2:g.119929841G>C GRCh38
NC_000023.10:g.119063804G>C , CM000685.1:g.119063804G>C GRCh37
NC_000023.9:g.118947832G>C NCBI36
NG_021260.1:g.18932C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1073+175C>G MANE Select ENSP00000360464.3:n.1073+175C>G
ENST00000652253.1:c.1069+175C>G
ENST00000371410.4:c.1073+175C>G ENSP00000360464.3:n.1073+175C>G
ENST00000477789.5:n.2001+175C>G
NM_024528.3:c.1073+175C>G NP_078804.2:n.1073+175C>G
XM_017029842.1:c.776+175C>G XP_016885331.1:n.776+175C>G
NM_024528.4:c.1073+175C>G MANE Select NP_078804.2:n.1073+175C>G
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