Canonical Allele Identifier: CA2206912502

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180131C= , CM000678.2:g.10180131C=	GRCh38
NC_000016.9:g.10273988C= , CM000678.1:g.10273988C=	GRCh37
NC_000016.8:g.10181489C=	NCBI36
NG_011812.1:g.7624G=
NG_011812.2:g.7624G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.281G= MANE Select	ENSP00000332549.3:p.Arg94=
ENST00000675189.1:n.765G=
ENST00000675398.1:c.281G=	ENSP00000502752.1:p.Arg94=
ENST00000676032.1:n.714G=
ENST00000330684.3:c.281G=	ENSP00000332549.3:p.Arg94=
ENST00000396573.6:c.281G=	ENSP00000379818.2:p.Arg94=
ENST00000562109.5:c.281G=	ENSP00000454998.1:p.Arg94=
ENST00000566665.1:n.682G=
NM_000833.4:c.281G=	NP_000824.1:p.Arg94=
NM_001134407.2:c.281G=	NP_001127879.1:p.Arg94=
NM_001134408.2:c.281G=	NP_001127880.1:p.Arg94=
XM_011522461.1:c.281G=	XP_011520763.1:p.Arg94=
XM_011522461.3:c.281G=	XP_011520763.1:p.Arg94=
XM_017023172.1:c.437G=	XP_016878661.1:p.Arg146=
XM_017023173.1:c.437G=	XP_016878662.1:p.Arg146=
NM_001134407.3:c.281G= MANE Select	NP_001127879.1:p.Arg94=
NM_000833.5:c.281G=	NP_000824.1:p.Arg94=