Canonical Allele Identifier: CA974532184
Gene: GRIN2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9764200del , CM000678.2:g.9764200del GRCh38
NC_000016.9:g.9858057del , CM000678.1:g.9858057del GRCh37
NC_000016.8:g.9765558del NCBI36
NG_011812.1:g.423555del
NG_011812.2:g.423555del

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.3344del MANE Select ENSP00000332549.3:p.Asp1115AlafsTer6
ENST00000535259.6:c.2873del ENSP00000441572.3:p.Asp958AlafsTer6
ENST00000636273.2:n.2937del
ENST00000674742.1:c.2873del ENSP00000502200.1:p.Asp958AlafsTer6
ENST00000675398.1:c.*714del ENSP00000502752.1:n.*714del
ENST00000330684.3:c.3344del ENSP00000332549.3:p.Asp1115AlafsTer6
ENST00000396573.6:c.3344del ENSP00000379818.2:p.Asp1115AlafsTer6
ENST00000396575.6:c.2933del ENSP00000379820.3:p.Asp978AlafsTer6
ENST00000461292.3:n.2983del
ENST00000535259.5:c.2933del ENSP00000441572.2:p.Asp978AlafsTer6
ENST00000562109.5:c.3344del ENSP00000454998.1:p.Asp1115AlafsTer6
NM_000833.4:c.3344del NP_000824.1:p.Asp1115AlafsTer6
NM_001134407.2:c.3344del NP_001127879.1:p.Asp1115AlafsTer6
NM_001134408.2:c.3344del NP_001127880.1:p.Asp1115AlafsTer6
XM_011522456.1:c.3185del XP_011520758.1:p.Asp1062AlafsTer6
XM_011522457.1:c.3086del XP_011520759.1:p.Asp1029AlafsTer6
XM_011522458.1:c.2873del XP_011520760.1:p.Asp958AlafsTer6
XM_011522459.1:c.2873del XP_011520761.1:p.Asp958AlafsTer6
XM_011522460.1:c.2873del XP_011520762.1:p.Asp958AlafsTer6
XM_011522461.1:c.3344del XP_011520763.1:p.Asp1115AlafsTer6
XM_011522458.3:c.2873del XP_011520760.1:p.Asp958AlafsTer6
XM_011522461.3:c.3344del XP_011520763.1:p.Asp1115AlafsTer6
XM_017023172.1:c.3500del XP_016878661.1:p.Asp1167AlafsTer6
XM_017023173.1:c.3500del XP_016878662.1:p.Asp1167AlafsTer6
NM_001134407.3:c.3344del MANE Select NP_001127879.1:p.Asp1115AlafsTer6
NM_000833.5:c.3344del NP_000824.1:p.Asp1115AlafsTer6