Canonical Allele Identifier: CA2206693114

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764207G= , CM000678.2:g.9764207G=	GRCh38
NC_000016.9:g.9858064G= , CM000678.1:g.9858064G=	GRCh37
NC_000016.8:g.9765565G=	NCBI36
NG_011812.1:g.423548C=
NG_011812.2:g.423548C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.3337C= MANE Select	ENSP00000332549.3:p.Pro1113=
ENST00000535259.6:c.2866C=	ENSP00000441572.3:p.Pro956=
ENST00000636273.2:n.2930C=
ENST00000674742.1:c.2866C=	ENSP00000502200.1:p.Pro956=
ENST00000675398.1:c.*707C=	ENSP00000502752.1:n.*707C=
ENST00000330684.3:c.3337C=	ENSP00000332549.3:p.Pro1113=
ENST00000396573.6:c.3337C=	ENSP00000379818.2:p.Pro1113=
ENST00000396575.6:c.2926C=	ENSP00000379820.3:p.Pro976=
ENST00000461292.3:n.2976C=
ENST00000535259.5:c.2926C=	ENSP00000441572.2:p.Pro976=
ENST00000562109.5:c.3337C=	ENSP00000454998.1:p.Pro1113=
NM_000833.4:c.3337C=	NP_000824.1:p.Pro1113=
NM_001134407.2:c.3337C=	NP_001127879.1:p.Pro1113=
NM_001134408.2:c.3337C=	NP_001127880.1:p.Pro1113=
XM_011522456.1:c.3178C=	XP_011520758.1:p.Pro1060=
XM_011522457.1:c.3079C=	XP_011520759.1:p.Pro1027=
XM_011522458.1:c.2866C=	XP_011520760.1:p.Pro956=
XM_011522459.1:c.2866C=	XP_011520761.1:p.Pro956=
XM_011522460.1:c.2866C=	XP_011520762.1:p.Pro956=
XM_011522461.1:c.3337C=	XP_011520763.1:p.Pro1113=
XM_011522458.3:c.2866C=	XP_011520760.1:p.Pro956=
XM_011522461.3:c.3337C=	XP_011520763.1:p.Pro1113=
XM_017023172.1:c.3493C=	XP_016878661.1:p.Pro1165=
XM_017023173.1:c.3493C=	XP_016878662.1:p.Pro1165=
NM_001134407.3:c.3337C= MANE Select	NP_001127879.1:p.Pro1113=
NM_000833.5:c.3337C=	NP_000824.1:p.Pro1113=