Canonical Allele Identifier: CA2425928129

Gene: NYX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41474587C= , CM000685.2:g.41474587C=	GRCh38
NC_000023.10:g.41333840C= , CM000685.1:g.41333840C=	GRCh37
NC_000023.9:g.41218784C=	NCBI36
NG_009112.1:g.32128C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.1119C=	ENSP00000340328.3:p.Phe373=
ENST00000378220.3:c.1119C= MANE Select	ENSP00000367465.2:p.Phe373=
ENST00000378220.2:c.1134C=	ENSP00000367465.1:p.Phe378=
ENST00000342595.2:c.1134C=	ENSP00000340328.2:p.Phe378=
ENST00000378220.1:c.1134C=	ENSP00000367465.1:p.Phe378=
NM_022567.2:c.1134C=	NP_072089.1:p.Phe378=
XM_005272632.2:c.1134C=	XP_005272689.1:p.Phe378=
XM_017029709.1:c.1134C=	XP_016885198.1:p.Phe378=
NM_001378477.3:c.1119C= MANE Select	NP_001365406.2:p.Phe373=
NM_022567.3:c.1119C=	NP_072089.2:p.Phe373=