Canonical Allele Identifier: CA2425928128

Gene: NYX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41474586T= , CM000685.2:g.41474586T=	GRCh38
NC_000023.10:g.41333839T= , CM000685.1:g.41333839T=	GRCh37
NC_000023.9:g.41218783T=	NCBI36
NG_009112.1:g.32127T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.1118T=	ENSP00000340328.3:p.Phe373=
ENST00000378220.3:c.1118T= MANE Select	ENSP00000367465.2:p.Phe373=
ENST00000378220.2:c.1133T=	ENSP00000367465.1:p.Phe378=
ENST00000342595.2:c.1133T=	ENSP00000340328.2:p.Phe378=
ENST00000378220.1:c.1133T=	ENSP00000367465.1:p.Phe378=
NM_022567.2:c.1133T=	NP_072089.1:p.Phe378=
XM_005272632.2:c.1133T=	XP_005272689.1:p.Phe378=
XM_017029709.1:c.1133T=	XP_016885198.1:p.Phe378=
NM_001378477.3:c.1118T= MANE Select	NP_001365406.2:p.Phe373=
NM_022567.3:c.1118T=	NP_072089.2:p.Phe373=