Canonical Allele Identifier: CA915951045
Gene: NYX HGNC NCBI

Linked Data

ClinVar Variation Id: 812362
ClinVar RCV Id: RCV001003103
dbSNP Id: rs1602181253
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41474714_41474715dup , CM000685.2:g.41474714_41474715dup GRCh38
NC_000023.10:g.41333967_41333968dup , CM000685.1:g.41333967_41333968dup GRCh37
NC_000023.9:g.41218911_41218912dup NCBI36
NG_009112.1:g.32255_32256dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000342595.3:c.1246_1247dup ENSP00000340328.3:p.Ala417TrpfsTer?
ENST00000378220.3:c.1246_1247dup MANE Select ENSP00000367465.2:p.Ala417TrpfsTer?
ENST00000378220.2:c.1261_1262dup ENSP00000367465.1:p.Ala422TrpfsTer?
ENST00000342595.2:c.1261_1262dup ENSP00000340328.2:p.Ala422TrpfsTer?
ENST00000378220.1:c.1261_1262dup ENSP00000367465.1:p.Ala422TrpfsTer?
NM_022567.2:c.1261_1262dup NP_072089.1:p.Ala422TrpfsTer?
XM_005272632.2:c.1261_1262dup XP_005272689.1:p.Ala422TrpfsTer?
XM_017029709.1:c.1261_1262dup XP_016885198.1:p.Ala422TrpfsTer?
NM_001378477.3:c.1246_1247dup MANE Select NP_001365406.2:p.Ala417TrpfsTer?
NM_022567.3:c.1246_1247dup NP_072089.2:p.Ala417TrpfsTer?
Search 100 bp 5'
Search 100 bp 3'