Canonical Allele Identifier: CA2206692766

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763534G= , CM000678.2:g.9763534G=	GRCh38
NC_000016.9:g.9857391G= , CM000678.1:g.9857391G=	GRCh37
NC_000016.8:g.9764892G=	NCBI36
NG_011812.1:g.424221C=
NG_011812.2:g.424221C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4010C= MANE Select	ENSP00000332549.3:p.Ser1337=
ENST00000535259.6:c.3302-106C=	ENSP00000441572.3:n.3302-106C=
ENST00000636273.2:n.3366-106C=
ENST00000674742.1:c.3539C=	ENSP00000502200.1:p.Ser1180=
ENST00000675398.1:c.*1380C=	ENSP00000502752.1:n.*1380C=
ENST00000330684.3:c.4010C=	ENSP00000332549.3:p.Ser1337=
ENST00000396573.6:c.4010C=	ENSP00000379818.2:p.Ser1337=
ENST00000396575.6:c.3599C=	ENSP00000379820.3:p.Ser1200=
ENST00000461292.3:n.3412-106C=
ENST00000535259.5:c.3362-106C=	ENSP00000441572.2:n.3362-106C=
ENST00000562109.5:c.3773-106C=	ENSP00000454998.1:n.3773-106C=
NM_000833.4:c.4010C=	NP_000824.1:p.Ser1337=
NM_001134407.2:c.4010C=	NP_001127879.1:p.Ser1337=
NM_001134408.2:c.3773-106C=	NP_001127880.1:n.3773-106C=
XM_011522456.1:c.3851C=	XP_011520758.1:p.Ser1284=
XM_011522457.1:c.3752C=	XP_011520759.1:p.Ser1251=
XM_011522458.1:c.3539C=	XP_011520760.1:p.Ser1180=
XM_011522459.1:c.3539C=	XP_011520761.1:p.Ser1180=
XM_011522460.1:c.3539C=	XP_011520762.1:p.Ser1180=
XM_011522461.1:c.3773-106C=	XP_011520763.1:n.3773-106C=
XM_011522458.3:c.3539C=	XP_011520760.1:p.Ser1180=
XM_011522461.3:c.3773-106C=	XP_011520763.1:n.3773-106C=
XM_017023172.1:c.4166C=	XP_016878661.1:p.Ser1389=
XM_017023173.1:c.3929-106C=	XP_016878662.1:n.3929-106C=
NM_001134407.3:c.4010C= MANE Select	NP_001127879.1:p.Ser1337=
NM_000833.5:c.4010C=	NP_000824.1:p.Ser1337=