Canonical Allele Identifier: CA2694579752
Gene: NKAP HGNC NCBI

Linked Data

gnomAD v4: X-119929951-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119929951T>G , CM000685.2:g.119929951T>G GRCh38
NC_000023.10:g.119063914T>G , CM000685.1:g.119063914T>G GRCh37
NC_000023.9:g.118947942T>G NCBI36
NG_021260.1:g.18822A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.1073+65A>C MANE Select ENSP00000360464.3:n.1073+65A>C
ENST00000652253.1:c.1069+65A>C
ENST00000371410.4:c.1073+65A>C ENSP00000360464.3:n.1073+65A>C
ENST00000477789.5:n.2001+65A>C
NM_024528.3:c.1073+65A>C NP_078804.2:n.1073+65A>C
XM_017029842.1:c.776+65A>C XP_016885331.1:n.776+65A>C
NM_024528.4:c.1073+65A>C MANE Select NP_078804.2:n.1073+65A>C
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