Canonical Allele Identifier: CA412992656

Gene: NYX

Linked Data

• gnomAD v4: X-41474565-T-C
• MyVariant Identifiers: chrX:g.41333818T>C (hg19) ; chrX:g.41474565T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41474565T>C , CM000685.2:g.41474565T>C	GRCh38
NC_000023.10:g.41333818T>C , CM000685.1:g.41333818T>C	GRCh37
NC_000023.9:g.41218762T>C	NCBI36
NG_009112.1:g.32106T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.1097T>C	ENSP00000340328.3:p.Leu366Pro
ENST00000378220.3:c.1097T>C MANE Select	ENSP00000367465.2:p.Leu366Pro
ENST00000378220.2:c.1112T>C	ENSP00000367465.1:p.Leu371Pro
ENST00000342595.2:c.1112T>C	ENSP00000340328.2:p.Leu371Pro
ENST00000378220.1:c.1112T>C	ENSP00000367465.1:p.Leu371Pro
NM_022567.2:c.1112T>C	NP_072089.1:p.Leu371Pro
XM_005272632.2:c.1112T>C	XP_005272689.1:p.Leu371Pro
XM_017029709.1:c.1112T>C	XP_016885198.1:p.Leu371Pro
NM_001378477.3:c.1097T>C MANE Select	NP_001365406.2:p.Leu366Pro
NM_022567.3:c.1097T>C	NP_072089.2:p.Leu366Pro