Canonical Allele Identifier: CA412993135

Gene: NYX

Linked Data

• ClinVar Variation Id: 2794771
• ClinVar RCV Id: RCV003673039
• gnomAD v4: X-41474681-G-A
• MyVariant Identifiers: chrX:g.41333934G>A (hg19) ; chrX:g.41474681G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41474681G>A , CM000685.2:g.41474681G>A	GRCh38
NC_000023.10:g.41333934G>A , CM000685.1:g.41333934G>A	GRCh37
NC_000023.9:g.41218878G>A	NCBI36
NG_009112.1:g.32222G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.1213G>A	ENSP00000340328.3:p.Val405Met
ENST00000378220.3:c.1213G>A MANE Select	ENSP00000367465.2:p.Val405Met
ENST00000378220.2:c.1228G>A	ENSP00000367465.1:p.Val410Met
ENST00000342595.2:c.1228G>A	ENSP00000340328.2:p.Val410Met
ENST00000378220.1:c.1228G>A	ENSP00000367465.1:p.Val410Met
NM_022567.2:c.1228G>A	NP_072089.1:p.Val410Met
XM_005272632.2:c.1228G>A	XP_005272689.1:p.Val410Met
XM_017029709.1:c.1228G>A	XP_016885198.1:p.Val410Met
NM_001378477.3:c.1213G>A MANE Select	NP_001365406.2:p.Val405Met
NM_022567.3:c.1213G>A	NP_072089.2:p.Val405Met