Canonical Allele Identifier: CA412992483
Gene: NYX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474511G>A , CM000685.2:g.41474511G>A GRCh38
NC_000023.10:g.41333764G>A , CM000685.1:g.41333764G>A GRCh37
NC_000023.9:g.41218708G>A NCBI36
NG_009112.1:g.32052G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1043G>A ENSP00000340328.3:p.Gly348Asp
ENST00000378220.3:c.1043G>A MANE Select ENSP00000367465.2:p.Gly348Asp
ENST00000378220.2:c.1058G>A ENSP00000367465.1:p.Gly353Asp
ENST00000342595.2:c.1058G>A ENSP00000340328.2:p.Gly353Asp
ENST00000378220.1:c.1058G>A ENSP00000367465.1:p.Gly353Asp
NM_022567.2:c.1058G>A NP_072089.1:p.Gly353Asp
XM_005272632.2:c.1058G>A XP_005272689.1:p.Gly353Asp
XM_017029709.1:c.1058G>A XP_016885198.1:p.Gly353Asp
NM_001378477.3:c.1043G>A MANE Select NP_001365406.2:p.Gly348Asp
NM_022567.3:c.1043G>A NP_072089.2:p.Gly348Asp