Canonical Allele Identifier: CA2206782622

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938083C= , CM000678.2:g.9938083C=	GRCh38
NC_000016.9:g.10031940C= , CM000678.1:g.10031940C=	GRCh37
NC_000016.8:g.9939441C=	NCBI36
NG_011812.1:g.249672G=
NG_011812.2:g.249672G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.883G= MANE Select	ENSP00000332549.3:p.Gly295=
ENST00000535259.6:c.412G=	ENSP00000441572.3:p.Gly138=
ENST00000636273.2:n.476G=
ENST00000637393.1:c.475G=	ENSP00000490232.1:p.Gly159=
ENST00000674742.1:c.412G=	ENSP00000502200.1:p.Gly138=
ENST00000675189.1:n.1367G=
ENST00000675398.1:c.883G=	ENSP00000502752.1:p.Gly295=
ENST00000330684.3:c.883G=	ENSP00000332549.3:p.Gly295=
ENST00000396573.6:c.883G=	ENSP00000379818.2:p.Gly295=
ENST00000396575.6:c.472G=	ENSP00000379820.3:p.Gly158=
ENST00000461292.3:n.522G=
ENST00000535259.5:c.472G=	ENSP00000441572.2:p.Gly158=
ENST00000562109.5:c.883G=	ENSP00000454998.1:p.Gly295=
ENST00000566683.1:n.241-46983G=
ENST00000568247.3:n.775G=
NM_000833.4:c.883G=	NP_000824.1:p.Gly295=
NM_001134407.2:c.883G=	NP_001127879.1:p.Gly295=
NM_001134408.2:c.883G=	NP_001127880.1:p.Gly295=
XM_011522456.1:c.724G=	XP_011520758.1:p.Gly242=
XM_011522457.1:c.625G=	XP_011520759.1:p.Gly209=
XM_011522458.1:c.412G=	XP_011520760.1:p.Gly138=
XM_011522459.1:c.412G=	XP_011520761.1:p.Gly138=
XM_011522460.1:c.412G=	XP_011520762.1:p.Gly138=
XM_011522461.1:c.883G=	XP_011520763.1:p.Gly295=
XM_011522458.3:c.412G=	XP_011520760.1:p.Gly138=
XM_011522461.3:c.883G=	XP_011520763.1:p.Gly295=
XM_017023172.1:c.1039G=	XP_016878661.1:p.Gly347=
XM_017023173.1:c.1039G=	XP_016878662.1:p.Gly347=
NM_001134407.3:c.883G= MANE Select	NP_001127879.1:p.Gly295=
NM_000833.5:c.883G=	NP_000824.1:p.Gly295=