Canonical Allele Identifier: CA2695222772
Gene: GRIN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9764780del , CM000678.2:g.9764780del GRCh38
NC_000016.9:g.9858637del , CM000678.1:g.9858637del GRCh37
NC_000016.8:g.9766138del NCBI36
NG_011812.1:g.422975del
NG_011812.2:g.422975del

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.2764del MANE Select ENSP00000332549.3:p.Ala922LeufsTer20
ENST00000535259.6:c.2293del ENSP00000441572.3:p.Ala765LeufsTer20
ENST00000636273.2:n.2357del
ENST00000674742.1:c.2293del ENSP00000502200.1:p.Ala765LeufsTer20
ENST00000675398.1:c.*134del ENSP00000502752.1:n.*134del
ENST00000330684.3:c.2764del ENSP00000332549.3:p.Ala922LeufsTer20
ENST00000396573.6:c.2764del ENSP00000379818.2:p.Ala922LeufsTer20
ENST00000396575.6:c.2353del ENSP00000379820.3:p.Ala785LeufsTer20
ENST00000461292.3:n.2403del
ENST00000535259.5:c.2353del ENSP00000441572.2:p.Ala785LeufsTer20
ENST00000562109.5:c.2764del ENSP00000454998.1:p.Ala922LeufsTer20
NM_000833.4:c.2764del NP_000824.1:p.Ala922LeufsTer20
NM_001134407.2:c.2764del NP_001127879.1:p.Ala922LeufsTer20
NM_001134408.2:c.2764del NP_001127880.1:p.Ala922LeufsTer20
XM_011522456.1:c.2605del XP_011520758.1:p.Ala869LeufsTer20
XM_011522457.1:c.2506del XP_011520759.1:p.Ala836LeufsTer20
XM_011522458.1:c.2293del XP_011520760.1:p.Ala765LeufsTer20
XM_011522459.1:c.2293del XP_011520761.1:p.Ala765LeufsTer20
XM_011522460.1:c.2293del XP_011520762.1:p.Ala765LeufsTer20
XM_011522461.1:c.2764del XP_011520763.1:p.Ala922LeufsTer20
XM_011522458.3:c.2293del XP_011520760.1:p.Ala765LeufsTer20
XM_011522461.3:c.2764del XP_011520763.1:p.Ala922LeufsTer20
XM_017023172.1:c.2920del XP_016878661.1:p.Ala974LeufsTer20
XM_017023173.1:c.2920del XP_016878662.1:p.Ala974LeufsTer20
NM_001134407.3:c.2764del MANE Select NP_001127879.1:p.Ala922LeufsTer20
NM_000833.5:c.2764del NP_000824.1:p.Ala922LeufsTer20