Canonical Allele Identifier: CA518222049

Gene: NKAP

Linked Data

• MyVariant Identifiers: chrX:g.119064041A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119930078A>T , CM000685.2:g.119930078A>T	GRCh38
NC_000023.10:g.119064041A>T , CM000685.1:g.119064041A>T	GRCh37
NC_000023.9:g.118948069A>T	NCBI36
NG_021260.1:g.18695T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371410.5:c.1011T>A MANE Select	ENSP00000360464.3:p.Ile337=
ENST00000652253.1:c.1007T>A
ENST00000371410.4:c.1011T>A	ENSP00000360464.3:p.Ile337=
ENST00000477789.5:n.1939T>A
NM_024528.3:c.1011T>A	NP_078804.2:p.Ile337=
XM_017029842.1:c.714T>A	XP_016885331.1:p.Ile238=
NM_024528.4:c.1011T>A MANE Select	NP_078804.2:p.Ile337=