Canonical Allele Identifier: CA645509403

Gene: NYX

Linked Data

• ClinVar Variation Id: 438057
• ClinVar RCV Id: RCV000504858
• dbSNP Id: rs1555967281
• MyVariant Identifiers: chrX:g.41333704_41333709del (hg19) ; chrX:g.41474451_41474456del (hg38)
• PubMed: PMID:28041643

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41474451_41474456del , CM000685.2:g.41474451_41474456del	GRCh38
NC_000023.10:g.41333704_41333709del , CM000685.1:g.41333704_41333709del	GRCh37
NC_000023.9:g.41218648_41218653del	NCBI36
NG_009112.1:g.31992_31997del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.983_988del	ENSP00000340328.3:p.Leu328_Phe329del
ENST00000378220.3:c.983_988del MANE Select	ENSP00000367465.2:p.Leu328_Phe329del
ENST00000378220.2:c.998_1003del	ENSP00000367465.1:p.Leu333_Phe334del
ENST00000342595.2:c.998_1003del	ENSP00000340328.2:p.Leu333_Phe334del
ENST00000378220.1:c.998_1003del	ENSP00000367465.1:p.Leu333_Phe334del
NM_022567.2:c.998_1003del	NP_072089.1:p.Leu333_Phe334del
XM_005272632.2:c.998_1003del	XP_005272689.1:p.Leu333_Phe334del
XM_017029709.1:c.998_1003del	XP_016885198.1:p.Leu333_Phe334del
NM_001378477.3:c.983_988del MANE Select	NP_001365406.2:p.Leu328_Phe329del
NM_022567.3:c.983_988del	NP_072089.2:p.Leu328_Phe329del