Canonical Allele Identifier: CA2579588842
Gene: NYX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474613_41474614del , CM000685.2:g.41474613_41474614del GRCh38
NC_000023.10:g.41333866_41333867del , CM000685.1:g.41333866_41333867del GRCh37
NC_000023.9:g.41218810_41218811del NCBI36
NG_009112.1:g.32154_32155del

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1145_1146del ENSP00000340328.3:p.Val382GlyfsTer?
ENST00000378220.3:c.1145_1146del MANE Select ENSP00000367465.2:p.Val382GlyfsTer?
ENST00000378220.2:c.1160_1161del ENSP00000367465.1:p.Val387GlyfsTer?
ENST00000342595.2:c.1160_1161del ENSP00000340328.2:p.Val387GlyfsTer?
ENST00000378220.1:c.1160_1161del ENSP00000367465.1:p.Val387GlyfsTer?
NM_022567.2:c.1160_1161del NP_072089.1:p.Val387GlyfsTer?
XM_005272632.2:c.1160_1161del XP_005272689.1:p.Val387GlyfsTer?
XM_017029709.1:c.1160_1161del XP_016885198.1:p.Val387GlyfsTer?
NM_001378477.3:c.1145_1146del MANE Select NP_001365406.2:p.Val382GlyfsTer?
NM_022567.3:c.1145_1146del NP_072089.2:p.Val382GlyfsTer?