Canonical Allele Identifier: CA412992728
Gene: NYX HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.41333833T>A (hg19) chrX:g.41474580T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474580T>A , CM000685.2:g.41474580T>A GRCh38
NC_000023.10:g.41333833T>A , CM000685.1:g.41333833T>A GRCh37
NC_000023.9:g.41218777T>A NCBI36
NG_009112.1:g.32121T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1112T>A ENSP00000340328.3:p.Val371Glu
ENST00000378220.3:c.1112T>A MANE Select ENSP00000367465.2:p.Val371Glu
ENST00000378220.2:c.1127T>A ENSP00000367465.1:p.Val376Glu
ENST00000342595.2:c.1127T>A ENSP00000340328.2:p.Val376Glu
ENST00000378220.1:c.1127T>A ENSP00000367465.1:p.Val376Glu
NM_022567.2:c.1127T>A NP_072089.1:p.Val376Glu
XM_005272632.2:c.1127T>A XP_005272689.1:p.Val376Glu
XM_017029709.1:c.1127T>A XP_016885198.1:p.Val376Glu
NM_001378477.3:c.1112T>A MANE Select NP_001365406.2:p.Val371Glu
NM_022567.3:c.1112T>A NP_072089.2:p.Val371Glu
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