Canonical Allele Identifier: CA227936

Gene: NYX

Linked Data

• ClinVar Variation Id: 11422
• ClinVar RCV Id: RCV000012175 ; RCV000086261
• dbSNP Id: rs62637021
• gnomAD v4: X-41473558-C-A
• MyVariant Identifiers: chrX:g.41332811C>A (hg19) ; chrX:g.41473558C>A (hg38)
• PubMed: PMID:11062472

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41473558C>A , CM000685.2:g.41473558C>A	GRCh38
NC_000023.10:g.41332811C>A , CM000685.1:g.41332811C>A	GRCh37
NC_000023.9:g.41217755C>A	NCBI36
NG_009112.1:g.31099C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.90C>A	ENSP00000340328.3:p.Cys30Ter
ENST00000378220.3:c.90C>A MANE Select	ENSP00000367465.2:p.Cys30Ter
ENST00000378220.2:c.105C>A	ENSP00000367465.1:p.Cys35Ter
ENST00000342595.2:c.105C>A	ENSP00000340328.2:p.Cys35Ter
ENST00000378220.1:c.105C>A	ENSP00000367465.1:p.Cys35Ter
ENST00000486842.1:n.343C>A
NM_022567.2:c.105C>A	NP_072089.1:p.Cys35Ter
XM_005272632.2:c.105C>A	XP_005272689.1:p.Cys35Ter
XM_017029709.1:c.105C>A	XP_016885198.1:p.Cys35Ter
NM_001378477.3:c.90C>A MANE Select	NP_001365406.2:p.Cys30Ter
NM_022567.3:c.90C>A	NP_072089.2:p.Cys30Ter