Canonical Allele Identifier: CA516366066

Gene: NYX

Linked Data

• gnomAD v4: X-41474602-T-C
• MyVariant Identifiers: chrX:g.41333855T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41474602T>C , CM000685.2:g.41474602T>C	GRCh38
NC_000023.10:g.41333855T>C , CM000685.1:g.41333855T>C	GRCh37
NC_000023.9:g.41218799T>C	NCBI36
NG_009112.1:g.32143T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.1134T>C	ENSP00000340328.3:p.Asp378=
ENST00000378220.3:c.1134T>C MANE Select	ENSP00000367465.2:p.Asp378=
ENST00000378220.2:c.1149T>C	ENSP00000367465.1:p.Asp383=
ENST00000342595.2:c.1149T>C	ENSP00000340328.2:p.Asp383=
ENST00000378220.1:c.1149T>C	ENSP00000367465.1:p.Asp383=
NM_022567.2:c.1149T>C	NP_072089.1:p.Asp383=
XM_005272632.2:c.1149T>C	XP_005272689.1:p.Asp383=
XM_017029709.1:c.1149T>C	XP_016885198.1:p.Asp383=
NM_001378477.3:c.1134T>C MANE Select	NP_001365406.2:p.Asp378=
NM_022567.3:c.1134T>C	NP_072089.2:p.Asp378=