Canonical Allele Identifier: CA2206782596

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938029T= , CM000678.2:g.9938029T=	GRCh38
NC_000016.9:g.10031886T= , CM000678.1:g.10031886T=	GRCh37
NC_000016.8:g.9939387T=	NCBI36
NG_011812.1:g.249726A=
NG_011812.2:g.249726A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.937A= MANE Select	ENSP00000332549.3:p.Ile313=
ENST00000535259.6:c.466A=	ENSP00000441572.3:p.Ile156=
ENST00000636273.2:n.530A=
ENST00000637393.1:c.529A=	ENSP00000490232.1:p.Ile177=
ENST00000674742.1:c.466A=	ENSP00000502200.1:p.Ile156=
ENST00000675189.1:n.1421A=
ENST00000675398.1:c.937A=	ENSP00000502752.1:p.Ile313=
ENST00000330684.3:c.937A=	ENSP00000332549.3:p.Ile313=
ENST00000396573.6:c.937A=	ENSP00000379818.2:p.Ile313=
ENST00000396575.6:c.526A=	ENSP00000379820.3:p.Ile176=
ENST00000461292.3:n.576A=
ENST00000535259.5:c.526A=	ENSP00000441572.2:p.Ile176=
ENST00000562109.5:c.937A=	ENSP00000454998.1:p.Ile313=
ENST00000566683.1:n.241-46929A=
ENST00000568247.3:n.829A=
NM_000833.4:c.937A=	NP_000824.1:p.Ile313=
NM_001134407.2:c.937A=	NP_001127879.1:p.Ile313=
NM_001134408.2:c.937A=	NP_001127880.1:p.Ile313=
XM_011522456.1:c.778A=	XP_011520758.1:p.Ile260=
XM_011522457.1:c.679A=	XP_011520759.1:p.Ile227=
XM_011522458.1:c.466A=	XP_011520760.1:p.Ile156=
XM_011522459.1:c.466A=	XP_011520761.1:p.Ile156=
XM_011522460.1:c.466A=	XP_011520762.1:p.Ile156=
XM_011522461.1:c.937A=	XP_011520763.1:p.Ile313=
XM_011522458.3:c.466A=	XP_011520760.1:p.Ile156=
XM_011522461.3:c.937A=	XP_011520763.1:p.Ile313=
XM_017023172.1:c.1093A=	XP_016878661.1:p.Ile365=
XM_017023173.1:c.1093A=	XP_016878662.1:p.Ile365=
NM_001134407.3:c.937A= MANE Select	NP_001127879.1:p.Ile313=
NM_000833.5:c.937A=	NP_000824.1:p.Ile313=