Canonical Allele Identifier: CA2206692709

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763415_9763416delinsAG , CM000678.2:g.9763415_9763416delinsAG	GRCh38
NC_000016.9:g.9857272_9857273delinsAG , CM000678.1:g.9857272_9857273delinsAG	GRCh37
NC_000016.8:g.9764773_9764774delinsAG	NCBI36
NG_011812.1:g.424339_424340delinsCT
NG_011812.2:g.424339_424340delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4128_4129delinsCT MANE Select	ENSP00000332549.3:p.Arg1376=
ENST00000535259.6:c.3314_3315delinsCT	ENSP00000441572.3:p.Ala1105=
ENST00000636273.2:n.3378_3379delinsCT
ENST00000674742.1:c.3657_3658delinsCT	ENSP00000502200.1:p.Arg1219=
ENST00000675398.1:c.*1498_*1499delinsCT	ENSP00000502752.1:n.*1498_*1499delinsCT
ENST00000330684.3:c.4128_4129delinsCT	ENSP00000332549.3:p.Arg1376=
ENST00000396573.6:c.4128_4129delinsCT	ENSP00000379818.2:p.Arg1376=
ENST00000396575.6:c.3717_3718delinsCT	ENSP00000379820.3:p.Arg1239=
ENST00000461292.3:n.3424_3425delinsCT
ENST00000535259.5:c.3374_3375delinsCT	ENSP00000441572.2:p.Ala1125=
ENST00000562109.5:c.3785_3786delinsCT	ENSP00000454998.1:p.Ala1262=
NM_000833.4:c.4128_4129delinsCT	NP_000824.1:p.Arg1376=
NM_001134407.2:c.4128_4129delinsCT	NP_001127879.1:p.Arg1376=
NM_001134408.2:c.3785_3786delinsCT	NP_001127880.1:p.Ala1262=
XM_011522456.1:c.3969_3970delinsCT	XP_011520758.1:p.Arg1323=
XM_011522457.1:c.3870_3871delinsCT	XP_011520759.1:p.Arg1290=
XM_011522458.1:c.3657_3658delinsCT	XP_011520760.1:p.Arg1219=
XM_011522459.1:c.3657_3658delinsCT	XP_011520761.1:p.Arg1219=
XM_011522460.1:c.3657_3658delinsCT	XP_011520762.1:p.Arg1219=
XM_011522461.1:c.3785_3786delinsCT	XP_011520763.1:p.Ala1262=
XM_011522458.3:c.3657_3658delinsCT	XP_011520760.1:p.Arg1219=
XM_011522461.3:c.3785_3786delinsCT	XP_011520763.1:p.Ala1262=
XM_017023172.1:c.4284_4285delinsCT	XP_016878661.1:p.Arg1428=
XM_017023173.1:c.3941_3942delinsCT	XP_016878662.1:p.Ala1314=
NM_001134407.3:c.4128_4129delinsCT MANE Select	NP_001127879.1:p.Arg1376=
NM_000833.5:c.4128_4129delinsCT	NP_000824.1:p.Arg1376=