Canonical Allele Identifier: CA2206693459

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764873G= , CM000678.2:g.9764873G=	GRCh38
NC_000016.9:g.9858730G= , CM000678.1:g.9858730G=	GRCh37
NC_000016.8:g.9766231G=	NCBI36
NG_011812.1:g.422882C=
NG_011812.2:g.422882C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.2671C= MANE Select	ENSP00000332549.3:p.Gln891=
ENST00000535259.6:c.2200C=	ENSP00000441572.3:p.Gln734=
ENST00000636273.2:n.2264C=
ENST00000674742.1:c.2200C=	ENSP00000502200.1:p.Gln734=
ENST00000675398.1:c.*41C=	ENSP00000502752.1:n.*41C=
ENST00000330684.3:c.2671C=	ENSP00000332549.3:p.Gln891=
ENST00000396573.6:c.2671C=	ENSP00000379818.2:p.Gln891=
ENST00000396575.6:c.2260C=	ENSP00000379820.3:p.Gln754=
ENST00000461292.3:n.2310C=
ENST00000463531.1:n.454C=
ENST00000535259.5:c.2260C=	ENSP00000441572.2:p.Gln754=
ENST00000562109.5:c.2671C=	ENSP00000454998.1:p.Gln891=
NM_000833.4:c.2671C=	NP_000824.1:p.Gln891=
NM_001134407.2:c.2671C=	NP_001127879.1:p.Gln891=
NM_001134408.2:c.2671C=	NP_001127880.1:p.Gln891=
XM_011522456.1:c.2512C=	XP_011520758.1:p.Gln838=
XM_011522457.1:c.2413C=	XP_011520759.1:p.Gln805=
XM_011522458.1:c.2200C=	XP_011520760.1:p.Gln734=
XM_011522459.1:c.2200C=	XP_011520761.1:p.Gln734=
XM_011522460.1:c.2200C=	XP_011520762.1:p.Gln734=
XM_011522461.1:c.2671C=	XP_011520763.1:p.Gln891=
XM_011522458.3:c.2200C=	XP_011520760.1:p.Gln734=
XM_011522461.3:c.2671C=	XP_011520763.1:p.Gln891=
XM_017023172.1:c.2827C=	XP_016878661.1:p.Gln943=
XM_017023173.1:c.2827C=	XP_016878662.1:p.Gln943=
NM_001134407.3:c.2671C= MANE Select	NP_001127879.1:p.Gln891=
NM_000833.5:c.2671C=	NP_000824.1:p.Gln891=