Canonical Allele Identifier: CA2425928161

Gene: NYX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41474655C= , CM000685.2:g.41474655C=	GRCh38
NC_000023.10:g.41333908C= , CM000685.1:g.41333908C=	GRCh37
NC_000023.9:g.41218852C=	NCBI36
NG_009112.1:g.32196C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.1187C=	ENSP00000340328.3:p.Pro396=
ENST00000378220.3:c.1187C= MANE Select	ENSP00000367465.2:p.Pro396=
ENST00000378220.2:c.1202C=	ENSP00000367465.1:p.Pro401=
ENST00000342595.2:c.1202C=	ENSP00000340328.2:p.Pro401=
ENST00000378220.1:c.1202C=	ENSP00000367465.1:p.Pro401=
NM_022567.2:c.1202C=	NP_072089.1:p.Pro401=
XM_005272632.2:c.1202C=	XP_005272689.1:p.Pro401=
XM_017029709.1:c.1202C=	XP_016885198.1:p.Pro401=
NM_001378477.3:c.1187C= MANE Select	NP_001365406.2:p.Pro396=
NM_022567.3:c.1187C=	NP_072089.2:p.Pro396=