Canonical Allele Identifier: CA2425928175

Gene: NYX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41474691_41474694delinsTCAG , CM000685.2:g.41474691_41474694delinsTCAG	GRCh38
NC_000023.10:g.41333944_41333947delinsTCAG , CM000685.1:g.41333944_41333947delinsTCAG	GRCh37
NC_000023.9:g.41218888_41218891delinsTCAG	NCBI36
NG_009112.1:g.32232_32235delinsTCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.1223_1226delinsTCAG	ENSP00000340328.3:p.Phe408=
ENST00000378220.3:c.1223_1226delinsTCAG MANE Select	ENSP00000367465.2:p.Phe408=
ENST00000378220.2:c.1238_1241delinsTCAG	ENSP00000367465.1:p.Phe413=
ENST00000342595.2:c.1238_1241delinsTCAG	ENSP00000340328.2:p.Phe413=
ENST00000378220.1:c.1238_1241delinsTCAG	ENSP00000367465.1:p.Phe413=
NM_022567.2:c.1238_1241delinsTCAG	NP_072089.1:p.Phe413=
XM_005272632.2:c.1238_1241delinsTCAG	XP_005272689.1:p.Phe413=
XM_017029709.1:c.1238_1241delinsTCAG	XP_016885198.1:p.Phe413=
NM_001378477.3:c.1223_1226delinsTCAG MANE Select	NP_001365406.2:p.Phe408=
NM_022567.3:c.1223_1226delinsTCAG	NP_072089.2:p.Phe408=