Canonical Allele Identifier: CA2206692815

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763635G= , CM000678.2:g.9763635G=	GRCh38
NC_000016.9:g.9857492G= , CM000678.1:g.9857492G=	GRCh37
NC_000016.8:g.9764993G=	NCBI36
NG_011812.1:g.424120C=
NG_011812.2:g.424120C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.3909C= MANE Select	ENSP00000332549.3:p.Asp1303=
ENST00000535259.6:c.3301+137C=	ENSP00000441572.3:n.3301+137C=
ENST00000636273.2:n.3365+137C=
ENST00000674742.1:c.3438C=	ENSP00000502200.1:p.Asp1146=
ENST00000675398.1:c.*1279C=	ENSP00000502752.1:n.*1279C=
ENST00000330684.3:c.3909C=	ENSP00000332549.3:p.Asp1303=
ENST00000396573.6:c.3909C=	ENSP00000379818.2:p.Asp1303=
ENST00000396575.6:c.3498C=	ENSP00000379820.3:p.Asp1166=
ENST00000461292.3:n.3411+137C=
ENST00000535259.5:c.3361+137C=	ENSP00000441572.2:n.3361+137C=
ENST00000562109.5:c.3772+137C=	ENSP00000454998.1:n.3772+137C=
NM_000833.4:c.3909C=	NP_000824.1:p.Asp1303=
NM_001134407.2:c.3909C=	NP_001127879.1:p.Asp1303=
NM_001134408.2:c.3772+137C=	NP_001127880.1:n.3772+137C=
XM_011522456.1:c.3750C=	XP_011520758.1:p.Asp1250=
XM_011522457.1:c.3651C=	XP_011520759.1:p.Asp1217=
XM_011522458.1:c.3438C=	XP_011520760.1:p.Asp1146=
XM_011522459.1:c.3438C=	XP_011520761.1:p.Asp1146=
XM_011522460.1:c.3438C=	XP_011520762.1:p.Asp1146=
XM_011522461.1:c.3772+137C=	XP_011520763.1:n.3772+137C=
XM_011522458.3:c.3438C=	XP_011520760.1:p.Asp1146=
XM_011522461.3:c.3772+137C=	XP_011520763.1:n.3772+137C=
XM_017023172.1:c.4065C=	XP_016878661.1:p.Asp1355=
XM_017023173.1:c.3928+137C=	XP_016878662.1:n.3928+137C=
NM_001134407.3:c.3909C= MANE Select	NP_001127879.1:p.Asp1303=
NM_000833.5:c.3909C=	NP_000824.1:p.Asp1303=