Canonical Allele Identifier: CA2694579804

Gene: NKAP

Linked Data

• gnomAD v4: X-119930215-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119930215_119930216insG , CM000685.2:g.119930215_119930216insG	GRCh38
NC_000023.10:g.119064178_119064179insG , CM000685.1:g.119064178_119064179insG	GRCh37
NC_000023.9:g.118948206_118948207insG	NCBI36
NG_021260.1:g.18557_18558insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371410.5:c.924-51_924-50insC MANE Select	ENSP00000360464.3:n.924-51_924-50insC
ENST00000652253.1:c.920-51_920-50insC
ENST00000371410.4:c.924-51_924-50insC	ENSP00000360464.3:n.924-51_924-50insC
ENST00000477789.5:n.1852-51_1852-50insC
ENST00000482407.1:n.723-51_723-50insC
NM_024528.3:c.924-51_924-50insC	NP_078804.2:n.924-51_924-50insC
XM_017029842.1:c.627-51_627-50insC	XP_016885331.1:n.627-51_627-50insC
NM_024528.4:c.924-51_924-50insC MANE Select	NP_078804.2:n.924-51_924-50insC