Canonical Allele Identifier: CA10389928
Gene: NYX HGNC NCBI

Linked Data

ClinVar Variation Id: 1170019
ClinVar RCV Id: RCV001521950 RCV001699803
dbSNP Id: rs149170016
ExAC: X:41333950 G / A
gnomAD v2: X-41333950-G-A
gnomAD v3: X-41474697-G-A
gnomAD v4: X-41474697-G-A
MyVariant Identifiers: chrX:g.41333950G>A (hg19) chrX:g.41474697G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474697G>A , CM000685.2:g.41474697G>A GRCh38
NC_000023.10:g.41333950G>A , CM000685.1:g.41333950G>A GRCh37
NC_000023.9:g.41218894G>A NCBI36
NG_009112.1:g.32238G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1229G>A ENSP00000340328.3:p.Ser410Asn
ENST00000378220.3:c.1229G>A MANE Select ENSP00000367465.2:p.Ser410Asn
ENST00000378220.2:c.1244G>A ENSP00000367465.1:p.Ser415Asn
ENST00000342595.2:c.1244G>A ENSP00000340328.2:p.Ser415Asn
ENST00000378220.1:c.1244G>A ENSP00000367465.1:p.Ser415Asn
NM_022567.2:c.1244G>A NP_072089.1:p.Ser415Asn
XM_005272632.2:c.1244G>A XP_005272689.1:p.Ser415Asn
XM_017029709.1:c.1244G>A XP_016885198.1:p.Ser415Asn
NM_001378477.3:c.1229G>A MANE Select NP_001365406.2:p.Ser410Asn
NM_022567.3:c.1229G>A NP_072089.2:p.Ser410Asn
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