Canonical Allele Identifier: CA2206693375

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764721C= , CM000678.2:g.9764721C=	GRCh38
NC_000016.9:g.9858578C= , CM000678.1:g.9858578C=	GRCh37
NC_000016.8:g.9766079C=	NCBI36
NG_011812.1:g.423034G=
NG_011812.2:g.423034G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.2823G= MANE Select	ENSP00000332549.3:p.Leu941=
ENST00000535259.6:c.2352G=	ENSP00000441572.3:p.Leu784=
ENST00000636273.2:n.2416G=
ENST00000674742.1:c.2352G=	ENSP00000502200.1:p.Leu784=
ENST00000675398.1:c.*193G=	ENSP00000502752.1:n.*193G=
ENST00000330684.3:c.2823G=	ENSP00000332549.3:p.Leu941=
ENST00000396573.6:c.2823G=	ENSP00000379818.2:p.Leu941=
ENST00000396575.6:c.2412G=	ENSP00000379820.3:p.Leu804=
ENST00000461292.3:n.2462G=
ENST00000535259.5:c.2412G=	ENSP00000441572.2:p.Leu804=
ENST00000562109.5:c.2823G=	ENSP00000454998.1:p.Leu941=
NM_000833.4:c.2823G=	NP_000824.1:p.Leu941=
NM_001134407.2:c.2823G=	NP_001127879.1:p.Leu941=
NM_001134408.2:c.2823G=	NP_001127880.1:p.Leu941=
XM_011522456.1:c.2664G=	XP_011520758.1:p.Leu888=
XM_011522457.1:c.2565G=	XP_011520759.1:p.Leu855=
XM_011522458.1:c.2352G=	XP_011520760.1:p.Leu784=
XM_011522459.1:c.2352G=	XP_011520761.1:p.Leu784=
XM_011522460.1:c.2352G=	XP_011520762.1:p.Leu784=
XM_011522461.1:c.2823G=	XP_011520763.1:p.Leu941=
XM_011522458.3:c.2352G=	XP_011520760.1:p.Leu784=
XM_011522461.3:c.2823G=	XP_011520763.1:p.Leu941=
XM_017023172.1:c.2979G=	XP_016878661.1:p.Leu993=
XM_017023173.1:c.2979G=	XP_016878662.1:p.Leu993=
NM_001134407.3:c.2823G= MANE Select	NP_001127879.1:p.Leu941=
NM_000833.5:c.2823G=	NP_000824.1:p.Leu941=