Canonical Allele Identifier: CA2206692696

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763391C= , CM000678.2:g.9763391C=	GRCh38
NC_000016.9:g.9857248C= , CM000678.1:g.9857248C=	GRCh37
NC_000016.8:g.9764749C=	NCBI36
NG_011812.1:g.424364G=
NG_011812.2:g.424364G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4153G= MANE Select	ENSP00000332549.3:p.Asp1385=
ENST00000535259.6:c.3339G=	ENSP00000441572.3:p.Arg1113=
ENST00000636273.2:n.3403G=
ENST00000674742.1:c.3682G=	ENSP00000502200.1:p.Asp1228=
ENST00000675398.1:c.*1523G=	ENSP00000502752.1:n.*1523G=
ENST00000330684.3:c.4153G=	ENSP00000332549.3:p.Asp1385=
ENST00000396573.6:c.4153G=	ENSP00000379818.2:p.Asp1385=
ENST00000396575.6:c.3742G=	ENSP00000379820.3:p.Asp1248=
ENST00000461292.3:n.3449G=
ENST00000535259.5:c.3399G=	ENSP00000441572.2:p.Arg1133=
ENST00000562109.5:c.3810G=	ENSP00000454998.1:p.Arg1270=
NM_000833.4:c.4153G=	NP_000824.1:p.Asp1385=
NM_001134407.2:c.4153G=	NP_001127879.1:p.Asp1385=
NM_001134408.2:c.3810G=	NP_001127880.1:p.Arg1270=
XM_011522456.1:c.3994G=	XP_011520758.1:p.Asp1332=
XM_011522457.1:c.3895G=	XP_011520759.1:p.Asp1299=
XM_011522458.1:c.3682G=	XP_011520760.1:p.Asp1228=
XM_011522459.1:c.3682G=	XP_011520761.1:p.Asp1228=
XM_011522460.1:c.3682G=	XP_011520762.1:p.Asp1228=
XM_011522461.1:c.3810G=	XP_011520763.1:p.Arg1270=
XM_011522458.3:c.3682G=	XP_011520760.1:p.Asp1228=
XM_011522461.3:c.3810G=	XP_011520763.1:p.Arg1270=
XM_017023172.1:c.4309G=	XP_016878661.1:p.Asp1437=
XM_017023173.1:c.3966G=	XP_016878662.1:p.Arg1322=
NM_001134407.3:c.4153G= MANE Select	NP_001127879.1:p.Asp1385=
NM_000833.5:c.4153G=	NP_000824.1:p.Asp1385=