Canonical Allele Identifier: CA2206782772

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938417G= , CM000678.2:g.9938417G=	GRCh38
NC_000016.9:g.10032274G= , CM000678.1:g.10032274G=	GRCh37
NC_000016.8:g.9939775G=	NCBI36
NG_011812.1:g.249338C=
NG_011812.2:g.249338C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.549C= MANE Select	ENSP00000332549.3:p.Phe183=
ENST00000535259.6:c.78C=	ENSP00000441572.3:p.Phe26=
ENST00000636273.2:n.142C=
ENST00000637393.1:c.141C=	ENSP00000490232.1:p.Phe47=
ENST00000674742.1:c.78C=	ENSP00000502200.1:p.Phe26=
ENST00000675189.1:n.1033C=
ENST00000675398.1:c.549C=	ENSP00000502752.1:p.Phe183=
ENST00000330684.3:c.549C=	ENSP00000332549.3:p.Phe183=
ENST00000396573.6:c.549C=	ENSP00000379818.2:p.Phe183=
ENST00000396575.6:c.138C=	ENSP00000379820.3:p.Phe46=
ENST00000461292.3:n.188C=
ENST00000535259.5:c.138C=	ENSP00000441572.2:p.Phe46=
ENST00000562109.5:c.549C=	ENSP00000454998.1:p.Phe183=
ENST00000566670.2:n.391C=
ENST00000566683.1:n.241-47317C=
ENST00000568247.3:n.441C=
NM_000833.4:c.549C=	NP_000824.1:p.Phe183=
NM_001134407.2:c.549C=	NP_001127879.1:p.Phe183=
NM_001134408.2:c.549C=	NP_001127880.1:p.Phe183=
XM_011522456.1:c.390C=	XP_011520758.1:p.Phe130=
XM_011522457.1:c.291C=	XP_011520759.1:p.Phe97=
XM_011522458.1:c.78C=	XP_011520760.1:p.Phe26=
XM_011522459.1:c.78C=	XP_011520761.1:p.Phe26=
XM_011522460.1:c.78C=	XP_011520762.1:p.Phe26=
XM_011522461.1:c.549C=	XP_011520763.1:p.Phe183=
XM_011522458.3:c.78C=	XP_011520760.1:p.Phe26=
XM_011522461.3:c.549C=	XP_011520763.1:p.Phe183=
XM_017023172.1:c.705C=	XP_016878661.1:p.Phe235=
XM_017023173.1:c.705C=	XP_016878662.1:p.Phe235=
NM_001134407.3:c.549C= MANE Select	NP_001127879.1:p.Phe183=
NM_000833.5:c.549C=	NP_000824.1:p.Phe183=