Canonical Allele Identifier: CA2206692803

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763617C= , CM000678.2:g.9763617C=	GRCh38
NC_000016.9:g.9857474C= , CM000678.1:g.9857474C=	GRCh37
NC_000016.8:g.9764975C=	NCBI36
NG_011812.1:g.424138G=
NG_011812.2:g.424138G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.3927G= MANE Select	ENSP00000332549.3:p.Arg1309=
ENST00000535259.6:c.3301+155G=	ENSP00000441572.3:n.3301+155G=
ENST00000636273.2:n.3365+155G=
ENST00000674742.1:c.3456G=	ENSP00000502200.1:p.Arg1152=
ENST00000675398.1:c.*1297G=	ENSP00000502752.1:n.*1297G=
ENST00000330684.3:c.3927G=	ENSP00000332549.3:p.Arg1309=
ENST00000396573.6:c.3927G=	ENSP00000379818.2:p.Arg1309=
ENST00000396575.6:c.3516G=	ENSP00000379820.3:p.Arg1172=
ENST00000461292.3:n.3411+155G=
ENST00000535259.5:c.3361+155G=	ENSP00000441572.2:n.3361+155G=
ENST00000562109.5:c.3772+155G=	ENSP00000454998.1:n.3772+155G=
NM_000833.4:c.3927G=	NP_000824.1:p.Arg1309=
NM_001134407.2:c.3927G=	NP_001127879.1:p.Arg1309=
NM_001134408.2:c.3772+155G=	NP_001127880.1:n.3772+155G=
XM_011522456.1:c.3768G=	XP_011520758.1:p.Arg1256=
XM_011522457.1:c.3669G=	XP_011520759.1:p.Arg1223=
XM_011522458.1:c.3456G=	XP_011520760.1:p.Arg1152=
XM_011522459.1:c.3456G=	XP_011520761.1:p.Arg1152=
XM_011522460.1:c.3456G=	XP_011520762.1:p.Arg1152=
XM_011522461.1:c.3772+155G=	XP_011520763.1:n.3772+155G=
XM_011522458.3:c.3456G=	XP_011520760.1:p.Arg1152=
XM_011522461.3:c.3772+155G=	XP_011520763.1:n.3772+155G=
XM_017023172.1:c.4083G=	XP_016878661.1:p.Arg1361=
XM_017023173.1:c.3928+155G=	XP_016878662.1:n.3928+155G=
NM_001134407.3:c.3927G= MANE Select	NP_001127879.1:p.Arg1309=
NM_000833.5:c.3927G=	NP_000824.1:p.Arg1309=