Canonical Allele Identifier: CA2694579772
Gene: NKAP HGNC NCBI

Linked Data

gnomAD v4: X-119929981-AATC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119929984_119929986del , CM000685.2:g.119929984_119929986del GRCh38
NC_000023.10:g.119063947_119063949del , CM000685.1:g.119063947_119063949del GRCh37
NC_000023.9:g.118947975_118947977del NCBI36
NG_021260.1:g.18789_18791del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.1073+32_1073+34del MANE Select ENSP00000360464.3:n.1073+32_1073+34del
ENST00000652253.1:c.1069+32_1069+34del
ENST00000371410.4:c.1073+32_1073+34del ENSP00000360464.3:n.1073+32_1073+34del
ENST00000477789.5:n.2001+32_2001+34del
NM_024528.3:c.1073+32_1073+34del NP_078804.2:n.1073+32_1073+34del
XM_017029842.1:c.776+32_776+34del XP_016885331.1:n.776+32_776+34del
NM_024528.4:c.1073+32_1073+34del MANE Select NP_078804.2:n.1073+32_1073+34del
Search 100 bp 5'
Search 100 bp 3'