Canonical Allele Identifier: CA10389920
Gene: NYX HGNC NCBI

Linked Data

ClinVar Variation Id: 2182751
ClinVar RCV Id: RCV002592173
dbSNP Id: rs746961966
ExAC: X:41333908 C / G
gnomAD v2: X-41333908-C-G
gnomAD v3: X-41474655-C-G
gnomAD v4: X-41474655-C-G
MyVariant Identifiers: chrX:g.41333908C>G (hg19) chrX:g.41474655C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474655C>G , CM000685.2:g.41474655C>G GRCh38
NC_000023.10:g.41333908C>G , CM000685.1:g.41333908C>G GRCh37
NC_000023.9:g.41218852C>G NCBI36
NG_009112.1:g.32196C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1187C>G ENSP00000340328.3:p.Pro396Arg
ENST00000378220.3:c.1187C>G MANE Select ENSP00000367465.2:p.Pro396Arg
ENST00000378220.2:c.1202C>G ENSP00000367465.1:p.Pro401Arg
ENST00000342595.2:c.1202C>G ENSP00000340328.2:p.Pro401Arg
ENST00000378220.1:c.1202C>G ENSP00000367465.1:p.Pro401Arg
NM_022567.2:c.1202C>G NP_072089.1:p.Pro401Arg
XM_005272632.2:c.1202C>G XP_005272689.1:p.Pro401Arg
XM_017029709.1:c.1202C>G XP_016885198.1:p.Pro401Arg
NM_001378477.3:c.1187C>G MANE Select NP_001365406.2:p.Pro396Arg
NM_022567.3:c.1187C>G NP_072089.2:p.Pro396Arg
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