Canonical Allele Identifier: CA2206693391

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764747C= , CM000678.2:g.9764747C=	GRCh38
NC_000016.9:g.9858604C= , CM000678.1:g.9858604C=	GRCh37
NC_000016.8:g.9766105C=	NCBI36
NG_011812.1:g.423008G=
NG_011812.2:g.423008G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.2797G= MANE Select	ENSP00000332549.3:p.Asp933=
ENST00000535259.6:c.2326G=	ENSP00000441572.3:p.Asp776=
ENST00000636273.2:n.2390G=
ENST00000674742.1:c.2326G=	ENSP00000502200.1:p.Asp776=
ENST00000675398.1:c.*167G=	ENSP00000502752.1:n.*167G=
ENST00000330684.3:c.2797G=	ENSP00000332549.3:p.Asp933=
ENST00000396573.6:c.2797G=	ENSP00000379818.2:p.Asp933=
ENST00000396575.6:c.2386G=	ENSP00000379820.3:p.Asp796=
ENST00000461292.3:n.2436G=
ENST00000535259.5:c.2386G=	ENSP00000441572.2:p.Asp796=
ENST00000562109.5:c.2797G=	ENSP00000454998.1:p.Asp933=
NM_000833.4:c.2797G=	NP_000824.1:p.Asp933=
NM_001134407.2:c.2797G=	NP_001127879.1:p.Asp933=
NM_001134408.2:c.2797G=	NP_001127880.1:p.Asp933=
XM_011522456.1:c.2638G=	XP_011520758.1:p.Asp880=
XM_011522457.1:c.2539G=	XP_011520759.1:p.Asp847=
XM_011522458.1:c.2326G=	XP_011520760.1:p.Asp776=
XM_011522459.1:c.2326G=	XP_011520761.1:p.Asp776=
XM_011522460.1:c.2326G=	XP_011520762.1:p.Asp776=
XM_011522461.1:c.2797G=	XP_011520763.1:p.Asp933=
XM_011522458.3:c.2326G=	XP_011520760.1:p.Asp776=
XM_011522461.3:c.2797G=	XP_011520763.1:p.Asp933=
XM_017023172.1:c.2953G=	XP_016878661.1:p.Asp985=
XM_017023173.1:c.2953G=	XP_016878662.1:p.Asp985=
NM_001134407.3:c.2797G= MANE Select	NP_001127879.1:p.Asp933=
NM_000833.5:c.2797G=	NP_000824.1:p.Asp933=