Canonical Allele Identifier: CA2959733552

Gene: NYX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41447833T>A , CM000685.2:g.41447833T>A	GRCh38
NC_000023.10:g.41307086T>A , CM000685.1:g.41307086T>A	GRCh37
NC_000023.9:g.41192030T>A	NCBI36
NG_009112.1:g.5374T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001378477.3:c.-56-16T>A MANE Select	NP_001365406.2:n.-56-16T>A
ENST00000378220.3:c.-56-16T>A MANE Select	ENSP00000367465.2:n.-56-16T>A
NM_022567.2:c.-57T>A	NP_072089.1:n.-57T>A
NM_022567.3:c.-72T>A	NP_072089.2:n.-72T>A
ENST00000342595.2:c.-57T>A	ENSP00000340328.2:n.-57T>A
ENST00000342595.3:c.-72T>A	ENSP00000340328.3:n.-72T>A
ENST00000378220.1:c.-41-16T>A	ENSP00000367465.1:n.-41-16T>A
ENST00000378220.2:c.-41-16T>A	ENSP00000367465.1:n.-41-16T>A
XM_005272632.2:c.-41-16T>A	XP_005272689.1:n.-41-16T>A
XM_017029709.1:c.-41-16T>A	XP_016885198.1:n.-41-16T>A