Canonical Allele Identifier: CA518222100

Gene: NKAP

Linked Data

• MyVariant Identifiers: chrX:g.119064113C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119930150C>A , CM000685.2:g.119930150C>A	GRCh38
NC_000023.10:g.119064113C>A , CM000685.1:g.119064113C>A	GRCh37
NC_000023.9:g.118948141C>A	NCBI36
NG_021260.1:g.18623G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371410.5:c.939G>T MANE Select	ENSP00000360464.3:p.Leu313=
ENST00000652253.1:c.935G>T
ENST00000371410.4:c.939G>T	ENSP00000360464.3:p.Leu313=
ENST00000477789.5:n.1867G>T
ENST00000482407.1:n.738G>T
NM_024528.3:c.939G>T	NP_078804.2:p.Leu313=
XM_017029842.1:c.642G>T	XP_016885331.1:p.Leu214=
NM_024528.4:c.939G>T MANE Select	NP_078804.2:p.Leu313=