Canonical Allele Identifier: CA412992975

Gene: NYX

Linked Data

• dbSNP Id: rs374504146
• gnomAD v3: X-41474639-A-G
• gnomAD v4: X-41474639-A-G
• MyVariant Identifiers: chrX:g.41333892A>G (hg19) ; chrX:g.41474639A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.1171A>G	ENSP00000340328.3:p.Thr391Ala
ENST00000378220.3:c.1171A>G MANE Select	ENSP00000367465.2:p.Thr391Ala
ENST00000378220.2:c.1186A>G	ENSP00000367465.1:p.Thr396Ala
ENST00000342595.2:c.1186A>G	ENSP00000340328.2:p.Thr396Ala
ENST00000378220.1:c.1186A>G	ENSP00000367465.1:p.Thr396Ala
NM_022567.2:c.1186A>G	NP_072089.1:p.Thr396Ala
XM_005272632.2:c.1186A>G	XP_005272689.1:p.Thr396Ala
XM_017029709.1:c.1186A>G	XP_016885198.1:p.Thr396Ala
NM_001378477.3:c.1171A>G MANE Select	NP_001365406.2:p.Thr391Ala
NM_022567.3:c.1171A>G	NP_072089.2:p.Thr391Ala