Canonical Allele Identifier: CA974532196
Gene: GRIN2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9764201del , CM000678.2:g.9764201del GRCh38
NC_000016.9:g.9858058del , CM000678.1:g.9858058del GRCh37
NC_000016.8:g.9765559del NCBI36
NG_011812.1:g.423554del
NG_011812.2:g.423554del

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.3343del MANE Select ENSP00000332549.3:p.Asp1115ThrfsTer6
ENST00000535259.6:c.2872del ENSP00000441572.3:p.Asp958ThrfsTer6
ENST00000636273.2:n.2936del
ENST00000674742.1:c.2872del ENSP00000502200.1:p.Asp958ThrfsTer6
ENST00000675398.1:c.*713del ENSP00000502752.1:n.*713del
ENST00000330684.3:c.3343del ENSP00000332549.3:p.Asp1115ThrfsTer6
ENST00000396573.6:c.3343del ENSP00000379818.2:p.Asp1115ThrfsTer6
ENST00000396575.6:c.2932del ENSP00000379820.3:p.Asp978ThrfsTer6
ENST00000461292.3:n.2982del
ENST00000535259.5:c.2932del ENSP00000441572.2:p.Asp978ThrfsTer6
ENST00000562109.5:c.3343del ENSP00000454998.1:p.Asp1115ThrfsTer6
NM_000833.4:c.3343del NP_000824.1:p.Asp1115ThrfsTer6
NM_001134407.2:c.3343del NP_001127879.1:p.Asp1115ThrfsTer6
NM_001134408.2:c.3343del NP_001127880.1:p.Asp1115ThrfsTer6
XM_011522456.1:c.3184del XP_011520758.1:p.Asp1062ThrfsTer6
XM_011522457.1:c.3085del XP_011520759.1:p.Asp1029ThrfsTer6
XM_011522458.1:c.2872del XP_011520760.1:p.Asp958ThrfsTer6
XM_011522459.1:c.2872del XP_011520761.1:p.Asp958ThrfsTer6
XM_011522460.1:c.2872del XP_011520762.1:p.Asp958ThrfsTer6
XM_011522461.1:c.3343del XP_011520763.1:p.Asp1115ThrfsTer6
XM_011522458.3:c.2872del XP_011520760.1:p.Asp958ThrfsTer6
XM_011522461.3:c.3343del XP_011520763.1:p.Asp1115ThrfsTer6
XM_017023172.1:c.3499del XP_016878661.1:p.Asp1167ThrfsTer6
XM_017023173.1:c.3499del XP_016878662.1:p.Asp1167ThrfsTer6
NM_001134407.3:c.3343del MANE Select NP_001127879.1:p.Asp1115ThrfsTer6
NM_000833.5:c.3343del NP_000824.1:p.Asp1115ThrfsTer6