Canonical Allele Identifier: CA2206782625

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938093T= , CM000678.2:g.9938093T=	GRCh38
NC_000016.9:g.10031950T= , CM000678.1:g.10031950T=	GRCh37
NC_000016.8:g.9939451T=	NCBI36
NG_011812.1:g.249662A=
NG_011812.2:g.249662A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.873A= MANE Select	ENSP00000332549.3:p.Arg291=
ENST00000535259.6:c.402A=	ENSP00000441572.3:p.Arg134=
ENST00000636273.2:n.466A=
ENST00000637393.1:c.465A=	ENSP00000490232.1:p.Arg155=
ENST00000674742.1:c.402A=	ENSP00000502200.1:p.Arg134=
ENST00000675189.1:n.1357A=
ENST00000675398.1:c.873A=	ENSP00000502752.1:p.Arg291=
ENST00000330684.3:c.873A=	ENSP00000332549.3:p.Arg291=
ENST00000396573.6:c.873A=	ENSP00000379818.2:p.Arg291=
ENST00000396575.6:c.462A=	ENSP00000379820.3:p.Arg154=
ENST00000461292.3:n.512A=
ENST00000535259.5:c.462A=	ENSP00000441572.2:p.Arg154=
ENST00000562109.5:c.873A=	ENSP00000454998.1:p.Arg291=
ENST00000566683.1:n.241-46993A=
ENST00000568247.3:n.765A=
NM_000833.4:c.873A=	NP_000824.1:p.Arg291=
NM_001134407.2:c.873A=	NP_001127879.1:p.Arg291=
NM_001134408.2:c.873A=	NP_001127880.1:p.Arg291=
XM_011522456.1:c.714A=	XP_011520758.1:p.Arg238=
XM_011522457.1:c.615A=	XP_011520759.1:p.Arg205=
XM_011522458.1:c.402A=	XP_011520760.1:p.Arg134=
XM_011522459.1:c.402A=	XP_011520761.1:p.Arg134=
XM_011522460.1:c.402A=	XP_011520762.1:p.Arg134=
XM_011522461.1:c.873A=	XP_011520763.1:p.Arg291=
XM_011522458.3:c.402A=	XP_011520760.1:p.Arg134=
XM_011522461.3:c.873A=	XP_011520763.1:p.Arg291=
XM_017023172.1:c.1029A=	XP_016878661.1:p.Arg343=
XM_017023173.1:c.1029A=	XP_016878662.1:p.Arg343=
NM_001134407.3:c.873A= MANE Select	NP_001127879.1:p.Arg291=
NM_000833.5:c.873A=	NP_000824.1:p.Arg291=