Canonical Allele Identifier: CA2206782758

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938396T= , CM000678.2:g.9938396T=	GRCh38
NC_000016.9:g.10032253T= , CM000678.1:g.10032253T=	GRCh37
NC_000016.8:g.9939754T=	NCBI36
NG_011812.1:g.249359A=
NG_011812.2:g.249359A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.570A= MANE Select	ENSP00000332549.3:p.Thr190=
ENST00000535259.6:c.99A=	ENSP00000441572.3:p.Thr33=
ENST00000636273.2:n.163A=
ENST00000637393.1:c.162A=	ENSP00000490232.1:p.Thr54=
ENST00000674742.1:c.99A=	ENSP00000502200.1:p.Thr33=
ENST00000675189.1:n.1054A=
ENST00000675398.1:c.570A=	ENSP00000502752.1:p.Thr190=
ENST00000330684.3:c.570A=	ENSP00000332549.3:p.Thr190=
ENST00000396573.6:c.570A=	ENSP00000379818.2:p.Thr190=
ENST00000396575.6:c.159A=	ENSP00000379820.3:p.Thr53=
ENST00000461292.3:n.209A=
ENST00000535259.5:c.159A=	ENSP00000441572.2:p.Thr53=
ENST00000562109.5:c.570A=	ENSP00000454998.1:p.Thr190=
ENST00000566670.2:n.412A=
ENST00000566683.1:n.241-47296A=
ENST00000568247.3:n.462A=
NM_000833.4:c.570A=	NP_000824.1:p.Thr190=
NM_001134407.2:c.570A=	NP_001127879.1:p.Thr190=
NM_001134408.2:c.570A=	NP_001127880.1:p.Thr190=
XM_011522456.1:c.411A=	XP_011520758.1:p.Thr137=
XM_011522457.1:c.312A=	XP_011520759.1:p.Thr104=
XM_011522458.1:c.99A=	XP_011520760.1:p.Thr33=
XM_011522459.1:c.99A=	XP_011520761.1:p.Thr33=
XM_011522460.1:c.99A=	XP_011520762.1:p.Thr33=
XM_011522461.1:c.570A=	XP_011520763.1:p.Thr190=
XM_011522458.3:c.99A=	XP_011520760.1:p.Thr33=
XM_011522461.3:c.570A=	XP_011520763.1:p.Thr190=
XM_017023172.1:c.726A=	XP_016878661.1:p.Thr242=
XM_017023173.1:c.726A=	XP_016878662.1:p.Thr242=
NM_001134407.3:c.570A= MANE Select	NP_001127879.1:p.Thr190=
NM_000833.5:c.570A=	NP_000824.1:p.Thr190=