Canonical Allele Identifier: CA414193446

Gene: NKAP

Linked Data

• MyVariant Identifiers: chrX:g.119064119A>T (hg19) ; chrX:g.119930156A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119930156A>T , CM000685.2:g.119930156A>T	GRCh38
NC_000023.10:g.119064119A>T , CM000685.1:g.119064119A>T	GRCh37
NC_000023.9:g.118948147A>T	NCBI36
NG_021260.1:g.18617T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371410.5:c.933T>A MANE Select	ENSP00000360464.3:p.His311Gln
ENST00000652253.1:c.929T>A
ENST00000371410.4:c.933T>A	ENSP00000360464.3:p.His311Gln
ENST00000477789.5:n.1861T>A
ENST00000482407.1:n.732T>A
NM_024528.3:c.933T>A	NP_078804.2:p.His311Gln
XM_017029842.1:c.636T>A	XP_016885331.1:p.His212Gln
NM_024528.4:c.933T>A MANE Select	NP_078804.2:p.His311Gln