Canonical Allele Identifier: CA414193444

Gene: NKAP

Linked Data

• MyVariant Identifiers: chrX:g.119064118C>G (hg19) ; chrX:g.119930155C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119930155C>G , CM000685.2:g.119930155C>G	GRCh38
NC_000023.10:g.119064118C>G , CM000685.1:g.119064118C>G	GRCh37
NC_000023.9:g.118948146C>G	NCBI36
NG_021260.1:g.18618G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371410.5:c.934G>C MANE Select	ENSP00000360464.3:p.Ala312Pro
ENST00000652253.1:c.930G>C
ENST00000371410.4:c.934G>C	ENSP00000360464.3:p.Ala312Pro
ENST00000477789.5:n.1862G>C
ENST00000482407.1:n.733G>C
NM_024528.3:c.934G>C	NP_078804.2:p.Ala312Pro
XM_017029842.1:c.637G>C	XP_016885331.1:p.Ala213Pro
NM_024528.4:c.934G>C MANE Select	NP_078804.2:p.Ala312Pro