Canonical Allele Identifier: CA2695233447

Gene: NYX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41474658_41474659insT , CM000685.2:g.41474658_41474659insT	GRCh38
NC_000023.10:g.41333911_41333912insT , CM000685.1:g.41333911_41333912insT	GRCh37
NC_000023.9:g.41218855_41218856insT	NCBI36
NG_009112.1:g.32199_32200insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.1190_1191insT	ENSP00000340328.3:p.Glu399ArgfsTer?
ENST00000378220.3:c.1190_1191insT MANE Select	ENSP00000367465.2:p.Glu399ArgfsTer?
ENST00000378220.2:c.1205_1206insT	ENSP00000367465.1:p.Glu404ArgfsTer?
ENST00000342595.2:c.1205_1206insT	ENSP00000340328.2:p.Glu404ArgfsTer?
ENST00000378220.1:c.1205_1206insT	ENSP00000367465.1:p.Glu404ArgfsTer?
NM_022567.2:c.1205_1206insT	NP_072089.1:p.Glu404ArgfsTer?
XM_005272632.2:c.1205_1206insT	XP_005272689.1:p.Glu404ArgfsTer?
XM_017029709.1:c.1205_1206insT	XP_016885198.1:p.Glu404ArgfsTer?
NM_001378477.3:c.1190_1191insT MANE Select	NP_001365406.2:p.Glu399ArgfsTer?
NM_022567.3:c.1190_1191insT	NP_072089.2:p.Glu399ArgfsTer?