Canonical Allele Identifier: CA2206693405

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764768G= , CM000678.2:g.9764768G=	GRCh38
NC_000016.9:g.9858625G= , CM000678.1:g.9858625G=	GRCh37
NC_000016.8:g.9766126G=	NCBI36
NG_011812.1:g.422987C=
NG_011812.2:g.422987C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.2776C= MANE Select	ENSP00000332549.3:p.Gln926=
ENST00000535259.6:c.2305C=	ENSP00000441572.3:p.Gln769=
ENST00000636273.2:n.2369C=
ENST00000674742.1:c.2305C=	ENSP00000502200.1:p.Gln769=
ENST00000675398.1:c.*146C=	ENSP00000502752.1:n.*146C=
ENST00000330684.3:c.2776C=	ENSP00000332549.3:p.Gln926=
ENST00000396573.6:c.2776C=	ENSP00000379818.2:p.Gln926=
ENST00000396575.6:c.2365C=	ENSP00000379820.3:p.Gln789=
ENST00000461292.3:n.2415C=
ENST00000535259.5:c.2365C=	ENSP00000441572.2:p.Gln789=
ENST00000562109.5:c.2776C=	ENSP00000454998.1:p.Gln926=
NM_000833.4:c.2776C=	NP_000824.1:p.Gln926=
NM_001134407.2:c.2776C=	NP_001127879.1:p.Gln926=
NM_001134408.2:c.2776C=	NP_001127880.1:p.Gln926=
XM_011522456.1:c.2617C=	XP_011520758.1:p.Gln873=
XM_011522457.1:c.2518C=	XP_011520759.1:p.Gln840=
XM_011522458.1:c.2305C=	XP_011520760.1:p.Gln769=
XM_011522459.1:c.2305C=	XP_011520761.1:p.Gln769=
XM_011522460.1:c.2305C=	XP_011520762.1:p.Gln769=
XM_011522461.1:c.2776C=	XP_011520763.1:p.Gln926=
XM_011522458.3:c.2305C=	XP_011520760.1:p.Gln769=
XM_011522461.3:c.2776C=	XP_011520763.1:p.Gln926=
XM_017023172.1:c.2932C=	XP_016878661.1:p.Gln978=
XM_017023173.1:c.2932C=	XP_016878662.1:p.Gln978=
NM_001134407.3:c.2776C= MANE Select	NP_001127879.1:p.Gln926=
NM_000833.5:c.2776C=	NP_000824.1:p.Gln926=