Canonical Allele Identifier: CA2541539070
Gene: NKAP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930065_119930066insTTTTTT , CM000685.2:g.119930065_119930066insTTTTTT GRCh38
NC_000023.10:g.119064028_119064029insTTTTTT , CM000685.1:g.119064028_119064029insTTTTTT GRCh37
NC_000023.9:g.118948056_118948057insTTTTTT NCBI36
NG_021260.1:g.18707_18708insAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.1023_1024insAAAAAA MANE Select ENSP00000360464.3:p.Ser341_Glu342insLysLys
ENST00000652253.1:c.1019_1020insAAAAAA
ENST00000371410.4:c.1023_1024insAAAAAA ENSP00000360464.3:p.Ser341_Glu342insLysLys
ENST00000477789.5:n.1951_1952insAAAAAA
NM_024528.3:c.1023_1024insAAAAAA NP_078804.2:p.Ser341_Glu342insLysLys
XM_017029842.1:c.726_727insAAAAAA XP_016885331.1:p.Ser242_Glu243insLysLys
NM_024528.4:c.1023_1024insAAAAAA MANE Select NP_078804.2:p.Ser341_Glu342insLysLys
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