Canonical Allele Identifier: CA2206692731

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763471A= , CM000678.2:g.9763471A=	GRCh38
NC_000016.9:g.9857328A= , CM000678.1:g.9857328A=	GRCh37
NC_000016.8:g.9764829A=	NCBI36
NG_011812.1:g.424284T=
NG_011812.2:g.424284T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4073T= MANE Select	ENSP00000332549.3:p.Leu1358=
ENST00000535259.6:c.3302-43T=	ENSP00000441572.3:n.3302-43T=
ENST00000636273.2:n.3366-43T=
ENST00000674742.1:c.3602T=	ENSP00000502200.1:p.Leu1201=
ENST00000675398.1:c.*1443T=	ENSP00000502752.1:n.*1443T=
ENST00000330684.3:c.4073T=	ENSP00000332549.3:p.Leu1358=
ENST00000396573.6:c.4073T=	ENSP00000379818.2:p.Leu1358=
ENST00000396575.6:c.3662T=	ENSP00000379820.3:p.Leu1221=
ENST00000461292.3:n.3412-43T=
ENST00000535259.5:c.3362-43T=	ENSP00000441572.2:n.3362-43T=
ENST00000562109.5:c.3773-43T=	ENSP00000454998.1:n.3773-43T=
NM_000833.4:c.4073T=	NP_000824.1:p.Leu1358=
NM_001134407.2:c.4073T=	NP_001127879.1:p.Leu1358=
NM_001134408.2:c.3773-43T=	NP_001127880.1:n.3773-43T=
XM_011522456.1:c.3914T=	XP_011520758.1:p.Leu1305=
XM_011522457.1:c.3815T=	XP_011520759.1:p.Leu1272=
XM_011522458.1:c.3602T=	XP_011520760.1:p.Leu1201=
XM_011522459.1:c.3602T=	XP_011520761.1:p.Leu1201=
XM_011522460.1:c.3602T=	XP_011520762.1:p.Leu1201=
XM_011522461.1:c.3773-43T=	XP_011520763.1:n.3773-43T=
XM_011522458.3:c.3602T=	XP_011520760.1:p.Leu1201=
XM_011522461.3:c.3773-43T=	XP_011520763.1:n.3773-43T=
XM_017023172.1:c.4229T=	XP_016878661.1:p.Leu1410=
XM_017023173.1:c.3929-43T=	XP_016878662.1:n.3929-43T=
NM_001134407.3:c.4073T= MANE Select	NP_001127879.1:p.Leu1358=
NM_000833.5:c.4073T=	NP_000824.1:p.Leu1358=