Canonical Allele Identifier: CA2694579792

Gene: NKAP

Linked Data

• gnomAD v4: X-119930193-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119930193G>A , CM000685.2:g.119930193G>A	GRCh38
NC_000023.10:g.119064156G>A , CM000685.1:g.119064156G>A	GRCh37
NC_000023.9:g.118948184G>A	NCBI36
NG_021260.1:g.18580C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371410.5:c.924-28C>T MANE Select	ENSP00000360464.3:n.924-28C>T
ENST00000652253.1:c.920-28C>T
ENST00000371410.4:c.924-28C>T	ENSP00000360464.3:n.924-28C>T
ENST00000477789.5:n.1852-28C>T
ENST00000482407.1:n.723-28C>T
NM_024528.3:c.924-28C>T	NP_078804.2:n.924-28C>T
XM_017029842.1:c.627-28C>T	XP_016885331.1:n.627-28C>T
NM_024528.4:c.924-28C>T MANE Select	NP_078804.2:n.924-28C>T