Canonical Allele Identifier: CA10389926
Gene: NYX HGNC NCBI

Linked Data

ClinVar Variation Id: 1504170
ClinVar RCV Id: RCV002025992
dbSNP Id: rs770813743
ExAC: X:41333944 TCAG / T
gnomAD v2: X-41333944-TCAG-T
gnomAD v3: X-41474691-TCAG-T
gnomAD v4: X-41474691-TCAG-T
MyVariant Identifiers: chrX:g.41333945_41333947del (hg19) chrX:g.41474692_41474694del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474696_41474698del , CM000685.2:g.41474696_41474698del GRCh38
NC_000023.10:g.41333949_41333951del , CM000685.1:g.41333949_41333951del GRCh37
NC_000023.9:g.41218893_41218895del NCBI36
NG_009112.1:g.32237_32239del

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1228_1230del ENSP00000340328.3:p.Ser410del
ENST00000378220.3:c.1228_1230del MANE Select ENSP00000367465.2:p.Ser410del
ENST00000378220.2:c.1243_1245del ENSP00000367465.1:p.Ser415del
ENST00000342595.2:c.1243_1245del ENSP00000340328.2:p.Ser415del
ENST00000378220.1:c.1243_1245del ENSP00000367465.1:p.Ser415del
NM_022567.2:c.1243_1245del NP_072089.1:p.Ser415del
XM_005272632.2:c.1243_1245del XP_005272689.1:p.Ser415del
XM_017029709.1:c.1243_1245del XP_016885198.1:p.Ser415del
NM_001378477.3:c.1228_1230del MANE Select NP_001365406.2:p.Ser410del
NM_022567.3:c.1228_1230del NP_072089.2:p.Ser410del
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