Canonical Allele Identifier: CA2206692633

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763261A= , CM000678.2:g.9763261A=	GRCh38
NC_000016.9:g.9857118A= , CM000678.1:g.9857118A=	GRCh37
NC_000016.8:g.9764619A=	NCBI36
NG_011812.1:g.424494T=
NG_011812.2:g.424494T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4283T= MANE Select	ENSP00000332549.3:p.Val1428=
ENST00000535259.6:c.*94T=	ENSP00000441572.3:n.*94T=
ENST00000636273.2:n.3533T=
ENST00000674742.1:c.3812T=	ENSP00000502200.1:p.Val1271=
ENST00000675398.1:c.*1653T=	ENSP00000502752.1:n.*1653T=
ENST00000330684.3:c.4283T=	ENSP00000332549.3:p.Val1428=
ENST00000396573.6:c.4283T=	ENSP00000379818.2:p.Val1428=
ENST00000396575.6:c.3872T=	ENSP00000379820.3:p.Val1291=
ENST00000461292.3:n.3579T=
ENST00000535259.5:c.*94T=	ENSP00000441572.2:n.*94T=
ENST00000562109.5:c.*94T=	ENSP00000454998.1:n.*94T=
NM_000833.4:c.4283T=	NP_000824.1:p.Val1428=
NM_001134407.2:c.4283T=	NP_001127879.1:p.Val1428=
NM_001134408.2:c.*94T=	NP_001127880.1:n.*94T=
XM_011522456.1:c.4124T=	XP_011520758.1:p.Val1375=
XM_011522457.1:c.4025T=	XP_011520759.1:p.Val1342=
XM_011522458.1:c.3812T=	XP_011520760.1:p.Val1271=
XM_011522459.1:c.3812T=	XP_011520761.1:p.Val1271=
XM_011522460.1:c.3812T=	XP_011520762.1:p.Val1271=
XM_011522461.1:c.*94T=	XP_011520763.1:n.*94T=
XM_011522458.3:c.3812T=	XP_011520760.1:p.Val1271=
XM_011522461.3:c.*94T=	XP_011520763.1:n.*94T=
XM_017023172.1:c.4439T=	XP_016878661.1:p.Val1480=
XM_017023173.1:c.*94T=	XP_016878662.1:n.*94T=
NM_001134407.3:c.4283T= MANE Select	NP_001127879.1:p.Val1428=
NM_000833.5:c.4283T=	NP_000824.1:p.Val1428=