Canonical Allele Identifier: CA2694579788
Gene: NKAP HGNC NCBI

Linked Data

gnomAD v4: X-119930180-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930180A>G , CM000685.2:g.119930180A>G GRCh38
NC_000023.10:g.119064143A>G , CM000685.1:g.119064143A>G GRCh37
NC_000023.9:g.118948171A>G NCBI36
NG_021260.1:g.18593T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.924-15T>C MANE Select ENSP00000360464.3:n.924-15T>C
ENST00000652253.1:c.920-15T>C
ENST00000371410.4:c.924-15T>C ENSP00000360464.3:n.924-15T>C
ENST00000477789.5:n.1852-15T>C
ENST00000482407.1:n.723-15T>C
NM_024528.3:c.924-15T>C NP_078804.2:n.924-15T>C
XM_017029842.1:c.627-15T>C XP_016885331.1:n.627-15T>C
NM_024528.4:c.924-15T>C MANE Select NP_078804.2:n.924-15T>C
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