Canonical Allele Identifier: CA412992740

Gene: NYX

Linked Data

• ClinVar Variation Id: 2790665
• ClinVar RCV Id: RCV003670006
• MyVariant Identifiers: chrX:g.41333836C>A (hg19) ; chrX:g.41474583C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41474583C>A , CM000685.2:g.41474583C>A	GRCh38
NC_000023.10:g.41333836C>A , CM000685.1:g.41333836C>A	GRCh37
NC_000023.9:g.41218780C>A	NCBI36
NG_009112.1:g.32124C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.1115C>A	ENSP00000340328.3:p.Thr372Asn
ENST00000378220.3:c.1115C>A MANE Select	ENSP00000367465.2:p.Thr372Asn
ENST00000378220.2:c.1130C>A	ENSP00000367465.1:p.Thr377Asn
ENST00000342595.2:c.1130C>A	ENSP00000340328.2:p.Thr377Asn
ENST00000378220.1:c.1130C>A	ENSP00000367465.1:p.Thr377Asn
NM_022567.2:c.1130C>A	NP_072089.1:p.Thr377Asn
XM_005272632.2:c.1130C>A	XP_005272689.1:p.Thr377Asn
XM_017029709.1:c.1130C>A	XP_016885198.1:p.Thr377Asn
NM_001378477.3:c.1115C>A MANE Select	NP_001365406.2:p.Thr372Asn
NM_022567.3:c.1115C>A	NP_072089.2:p.Thr372Asn