Canonical Allele Identifier: CA10389917

Gene: NYX

Linked Data

• ClinVar Variation Id: 1499111
• ClinVar RCV Id: RCV002010426
• dbSNP Id: rs374504146
• ExAC: X:41333892 A / T
• gnomAD v2: X-41333892-A-T
• gnomAD v4: X-41474639-A-T
• MyVariant Identifiers: chrX:g.41333892A>T (hg19) ; chrX:g.41474639A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41474639A>T , CM000685.2:g.41474639A>T	GRCh38
NC_000023.10:g.41333892A>T , CM000685.1:g.41333892A>T	GRCh37
NC_000023.9:g.41218836A>T	NCBI36
NG_009112.1:g.32180A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.1171A>T	ENSP00000340328.3:p.Thr391Ser
ENST00000378220.3:c.1171A>T MANE Select	ENSP00000367465.2:p.Thr391Ser
ENST00000378220.2:c.1186A>T	ENSP00000367465.1:p.Thr396Ser
ENST00000342595.2:c.1186A>T	ENSP00000340328.2:p.Thr396Ser
ENST00000378220.1:c.1186A>T	ENSP00000367465.1:p.Thr396Ser
NM_022567.2:c.1186A>T	NP_072089.1:p.Thr396Ser
XM_005272632.2:c.1186A>T	XP_005272689.1:p.Thr396Ser
XM_017029709.1:c.1186A>T	XP_016885198.1:p.Thr396Ser
NM_001378477.3:c.1171A>T MANE Select	NP_001365406.2:p.Thr391Ser
NM_022567.3:c.1171A>T	NP_072089.2:p.Thr391Ser