Canonical Allele Identifier: CA2206692743

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763499C= , CM000678.2:g.9763499C=	GRCh38
NC_000016.9:g.9857356C= , CM000678.1:g.9857356C=	GRCh37
NC_000016.8:g.9764857C=	NCBI36
NG_011812.1:g.424256G=
NG_011812.2:g.424256G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4045G= MANE Select	ENSP00000332549.3:p.Glu1349=
ENST00000535259.6:c.3302-71G=	ENSP00000441572.3:n.3302-71G=
ENST00000636273.2:n.3366-71G=
ENST00000674742.1:c.3574G=	ENSP00000502200.1:p.Glu1192=
ENST00000675398.1:c.*1415G=	ENSP00000502752.1:n.*1415G=
ENST00000330684.3:c.4045G=	ENSP00000332549.3:p.Glu1349=
ENST00000396573.6:c.4045G=	ENSP00000379818.2:p.Glu1349=
ENST00000396575.6:c.3634G=	ENSP00000379820.3:p.Glu1212=
ENST00000461292.3:n.3412-71G=
ENST00000535259.5:c.3362-71G=	ENSP00000441572.2:n.3362-71G=
ENST00000562109.5:c.3773-71G=	ENSP00000454998.1:n.3773-71G=
NM_000833.4:c.4045G=	NP_000824.1:p.Glu1349=
NM_001134407.2:c.4045G=	NP_001127879.1:p.Glu1349=
NM_001134408.2:c.3773-71G=	NP_001127880.1:n.3773-71G=
XM_011522456.1:c.3886G=	XP_011520758.1:p.Glu1296=
XM_011522457.1:c.3787G=	XP_011520759.1:p.Glu1263=
XM_011522458.1:c.3574G=	XP_011520760.1:p.Glu1192=
XM_011522459.1:c.3574G=	XP_011520761.1:p.Glu1192=
XM_011522460.1:c.3574G=	XP_011520762.1:p.Glu1192=
XM_011522461.1:c.3773-71G=	XP_011520763.1:n.3773-71G=
XM_011522458.3:c.3574G=	XP_011520760.1:p.Glu1192=
XM_011522461.3:c.3773-71G=	XP_011520763.1:n.3773-71G=
XM_017023172.1:c.4201G=	XP_016878661.1:p.Glu1401=
XM_017023173.1:c.3929-71G=	XP_016878662.1:n.3929-71G=
NM_001134407.3:c.4045G= MANE Select	NP_001127879.1:p.Glu1349=
NM_000833.5:c.4045G=	NP_000824.1:p.Glu1349=