Canonical Allele Identifier: CA2206723573

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9822217G= , CM000678.2:g.9822217G=	GRCh38
NC_000016.9:g.9916074G= , CM000678.1:g.9916074G=	GRCh37
NC_000016.8:g.9823575G=	NCBI36
NG_011812.1:g.365538C=
NG_011812.2:g.365538C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.2168+47C= MANE Select	ENSP00000332549.3:n.2168+47C=
ENST00000535259.6:c.1697+47C=	ENSP00000441572.3:n.1697+47C=
ENST00000636273.2:n.1761+47C=
ENST00000674742.1:c.1697+47C=	ENSP00000502200.1:n.1697+47C=
ENST00000675398.1:c.2168+47C=	ENSP00000502752.1:n.2168+47C=
ENST00000330684.3:c.2168+47C=	ENSP00000332549.3:n.2168+47C=
ENST00000396573.6:c.2168+47C=	ENSP00000379818.2:n.2168+47C=
ENST00000396575.6:c.1757+47C=	ENSP00000379820.3:n.1757+47C=
ENST00000461292.3:n.1807+47C=
ENST00000535259.5:c.1757+47C=	ENSP00000441572.2:n.1757+47C=
ENST00000562109.5:c.2168+47C=	ENSP00000454998.1:n.2168+47C=
NM_000833.4:c.2168+47C=	NP_000824.1:n.2168+47C=
NM_001134407.2:c.2168+47C=	NP_001127879.1:n.2168+47C=
NM_001134408.2:c.2168+47C=	NP_001127880.1:n.2168+47C=
XM_011522456.1:c.2009+47C=	XP_011520758.1:n.2009+47C=
XM_011522457.1:c.1910+47C=	XP_011520759.1:n.1910+47C=
XM_011522458.1:c.1697+47C=	XP_011520760.1:n.1697+47C=
XM_011522459.1:c.1697+47C=	XP_011520761.1:n.1697+47C=
XM_011522460.1:c.1697+47C=	XP_011520762.1:n.1697+47C=
XM_011522461.1:c.2168+47C=	XP_011520763.1:n.2168+47C=
XM_011522458.3:c.1697+47C=	XP_011520760.1:n.1697+47C=
XM_011522461.3:c.2168+47C=	XP_011520763.1:n.2168+47C=
XM_017023172.1:c.2324+47C=	XP_016878661.1:n.2324+47C=
XM_017023173.1:c.2324+47C=	XP_016878662.1:n.2324+47C=
NM_001134407.3:c.2168+47C= MANE Select	NP_001127879.1:n.2168+47C=
NM_000833.5:c.2168+47C=	NP_000824.1:n.2168+47C=