Canonical Allele Identifier: CA2425928153

Gene: NYX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41474639A= , CM000685.2:g.41474639A=	GRCh38
NC_000023.10:g.41333892A= , CM000685.1:g.41333892A=	GRCh37
NC_000023.9:g.41218836A=	NCBI36
NG_009112.1:g.32180A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.1171A=	ENSP00000340328.3:p.Thr391=
ENST00000378220.3:c.1171A= MANE Select	ENSP00000367465.2:p.Thr391=
ENST00000378220.2:c.1186A=	ENSP00000367465.1:p.Thr396=
ENST00000342595.2:c.1186A=	ENSP00000340328.2:p.Thr396=
ENST00000378220.1:c.1186A=	ENSP00000367465.1:p.Thr396=
NM_022567.2:c.1186A=	NP_072089.1:p.Thr396=
XM_005272632.2:c.1186A=	XP_005272689.1:p.Thr396=
XM_017029709.1:c.1186A=	XP_016885198.1:p.Thr396=
NM_001378477.3:c.1171A= MANE Select	NP_001365406.2:p.Thr391=
NM_022567.3:c.1171A=	NP_072089.2:p.Thr391=