Canonical Allele Identifier: CA412993042
Gene: NYX HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.41333910T>A (hg19) chrX:g.41474657T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474657T>A , CM000685.2:g.41474657T>A GRCh38
NC_000023.10:g.41333910T>A , CM000685.1:g.41333910T>A GRCh37
NC_000023.9:g.41218854T>A NCBI36
NG_009112.1:g.32198T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1189T>A ENSP00000340328.3:p.Ser397Thr
ENST00000378220.3:c.1189T>A MANE Select ENSP00000367465.2:p.Ser397Thr
ENST00000378220.2:c.1204T>A ENSP00000367465.1:p.Ser402Thr
ENST00000342595.2:c.1204T>A ENSP00000340328.2:p.Ser402Thr
ENST00000378220.1:c.1204T>A ENSP00000367465.1:p.Ser402Thr
NM_022567.2:c.1204T>A NP_072089.1:p.Ser402Thr
XM_005272632.2:c.1204T>A XP_005272689.1:p.Ser402Thr
XM_017029709.1:c.1204T>A XP_016885198.1:p.Ser402Thr
NM_001378477.3:c.1189T>A MANE Select NP_001365406.2:p.Ser397Thr
NM_022567.3:c.1189T>A NP_072089.2:p.Ser397Thr
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