Canonical Allele Identifier: CA2425928102

Gene: NYX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41474519_41474521delinsCGT , CM000685.2:g.41474519_41474521delinsCGT	GRCh38
NC_000023.10:g.41333772_41333774delinsCGT , CM000685.1:g.41333772_41333774delinsCGT	GRCh37
NC_000023.9:g.41218716_41218718delinsCGT	NCBI36
NG_009112.1:g.32060_32062delinsCGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.1051_1053delinsCGT	ENSP00000340328.3:p.Arg351=
ENST00000378220.3:c.1051_1053delinsCGT MANE Select	ENSP00000367465.2:p.Arg351=
ENST00000378220.2:c.1066_1068delinsCGT	ENSP00000367465.1:p.Arg356=
ENST00000342595.2:c.1066_1068delinsCGT	ENSP00000340328.2:p.Arg356=
ENST00000378220.1:c.1066_1068delinsCGT	ENSP00000367465.1:p.Arg356=
NM_022567.2:c.1066_1068delinsCGT	NP_072089.1:p.Arg356=
XM_005272632.2:c.1066_1068delinsCGT	XP_005272689.1:p.Arg356=
XM_017029709.1:c.1066_1068delinsCGT	XP_016885198.1:p.Arg356=
NM_001378477.3:c.1051_1053delinsCGT MANE Select	NP_001365406.2:p.Arg351=
NM_022567.3:c.1051_1053delinsCGT	NP_072089.2:p.Arg351=