Canonical Allele Identifier: CA201701
Gene: NYX HGNC NCBI

Linked Data

ClinVar Variation Id: 195374
ClinVar RCV Id: RCV000175939 RCV001166052 RCV001521173
dbSNP Id: rs34169326
ExAC: X:41333923 C / G
gnomAD v2: X-41333923-C-G
gnomAD v3: X-41474670-C-G
gnomAD v4: X-41474670-C-G
MyVariant Identifiers: chrX:g.41333923C>G (hg19) chrX:g.41474670C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474670C>G , CM000685.2:g.41474670C>G GRCh38
NC_000023.10:g.41333923C>G , CM000685.1:g.41333923C>G GRCh37
NC_000023.9:g.41218867C>G NCBI36
NG_009112.1:g.32211C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1202C>G ENSP00000340328.3:p.Ala401Gly
ENST00000378220.3:c.1202C>G MANE Select ENSP00000367465.2:p.Ala401Gly
ENST00000378220.2:c.1217C>G ENSP00000367465.1:p.Ala406Gly
ENST00000342595.2:c.1217C>G ENSP00000340328.2:p.Ala406Gly
ENST00000378220.1:c.1217C>G ENSP00000367465.1:p.Ala406Gly
NM_022567.2:c.1217C>G NP_072089.1:p.Ala406Gly
XM_005272632.2:c.1217C>G XP_005272689.1:p.Ala406Gly
XM_017029709.1:c.1217C>G XP_016885198.1:p.Ala406Gly
NM_001378477.3:c.1202C>G MANE Select NP_001365406.2:p.Ala401Gly
NM_022567.3:c.1202C>G NP_072089.2:p.Ala401Gly
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