Canonical Allele Identifier: CA2206726988

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9829467G= , CM000678.2:g.9829467G=	GRCh38
NC_000016.9:g.9923324G= , CM000678.1:g.9923324G=	GRCh37
NC_000016.8:g.9830825G=	NCBI36
NG_011812.1:g.358288C=
NG_011812.2:g.358288C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.1963C= MANE Select	ENSP00000332549.3:p.Gln655=
ENST00000535259.6:c.1492C=	ENSP00000441572.3:p.Gln498=
ENST00000636273.2:n.1556C=
ENST00000674742.1:c.1492C=	ENSP00000502200.1:p.Gln498=
ENST00000675398.1:c.1963C=	ENSP00000502752.1:p.Gln655=
ENST00000330684.3:c.1963C=	ENSP00000332549.3:p.Gln655=
ENST00000396573.6:c.1963C=	ENSP00000379818.2:p.Gln655=
ENST00000396575.6:c.1552C=	ENSP00000379820.3:p.Gln518=
ENST00000461292.3:n.1602C=
ENST00000535259.5:c.1552C=	ENSP00000441572.2:p.Gln518=
ENST00000562109.5:c.1963C=	ENSP00000454998.1:p.Gln655=
NM_000833.4:c.1963C=	NP_000824.1:p.Gln655=
NM_001134407.2:c.1963C=	NP_001127879.1:p.Gln655=
NM_001134408.2:c.1963C=	NP_001127880.1:p.Gln655=
XM_011522456.1:c.1804C=	XP_011520758.1:p.Gln602=
XM_011522457.1:c.1705C=	XP_011520759.1:p.Gln569=
XM_011522458.1:c.1492C=	XP_011520760.1:p.Gln498=
XM_011522459.1:c.1492C=	XP_011520761.1:p.Gln498=
XM_011522460.1:c.1492C=	XP_011520762.1:p.Gln498=
XM_011522461.1:c.1963C=	XP_011520763.1:p.Gln655=
XM_011522458.3:c.1492C=	XP_011520760.1:p.Gln498=
XM_011522461.3:c.1963C=	XP_011520763.1:p.Gln655=
XM_017023172.1:c.2119C=	XP_016878661.1:p.Gln707=
XM_017023173.1:c.2119C=	XP_016878662.1:p.Gln707=
NM_001134407.3:c.1963C= MANE Select	NP_001127879.1:p.Gln655=
NM_000833.5:c.1963C=	NP_000824.1:p.Gln655=