Canonical Allele Identifier: CA493692385

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.9857009A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763152A>T , CM000678.2:g.9763152A>T	GRCh38
NC_000016.9:g.9857009A>T , CM000678.1:g.9857009A>T	GRCh37
NC_000016.8:g.9764510A>T	NCBI36
NG_011812.1:g.424603T>A
NG_011812.2:g.424603T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4392T>A MANE Select	ENSP00000332549.3:p.Val1464=
ENST00000535259.6:c.*203T>A	ENSP00000441572.3:n.*203T>A
ENST00000636273.2:n.3642T>A
ENST00000674742.1:c.3921T>A	ENSP00000502200.1:p.Val1307=
ENST00000675398.1:c.*1762T>A	ENSP00000502752.1:n.*1762T>A
ENST00000330684.3:c.4392T>A	ENSP00000332549.3:p.Val1464=
ENST00000396573.6:c.4392T>A	ENSP00000379818.2:p.Val1464=
ENST00000396575.6:c.3981T>A	ENSP00000379820.3:p.Val1327=
ENST00000461292.3:n.3688T>A
ENST00000535259.5:c.*203T>A	ENSP00000441572.2:n.*203T>A
ENST00000562109.5:c.*203T>A	ENSP00000454998.1:n.*203T>A
NM_000833.4:c.4392T>A	NP_000824.1:p.Val1464=
NM_001134407.2:c.4392T>A	NP_001127879.1:p.Val1464=
NM_001134408.2:c.*203T>A	NP_001127880.1:n.*203T>A
XM_011522456.1:c.4233T>A	XP_011520758.1:p.Val1411=
XM_011522457.1:c.4134T>A	XP_011520759.1:p.Val1378=
XM_011522458.1:c.3921T>A	XP_011520760.1:p.Val1307=
XM_011522459.1:c.3921T>A	XP_011520761.1:p.Val1307=
XM_011522460.1:c.3921T>A	XP_011520762.1:p.Val1307=
XM_011522461.1:c.*203T>A	XP_011520763.1:n.*203T>A
XM_011522458.3:c.3921T>A	XP_011520760.1:p.Val1307=
XM_011522461.3:c.*203T>A	XP_011520763.1:n.*203T>A
XM_017023172.1:c.4548T>A	XP_016878661.1:p.Val1516=
XM_017023173.1:c.*203T>A	XP_016878662.1:n.*203T>A
NM_001134407.3:c.4392T>A MANE Select	NP_001127879.1:p.Val1464=
NM_000833.5:c.4392T>A	NP_000824.1:p.Val1464=