Canonical Allele Identifier: CA493692902

Gene: GRIN2A

Linked Data

• dbSNP Id: rs1376865696
• gnomAD v4: 16-9763617-C-T
• MyVariant Identifiers: chr16:g.9857474C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763617C>T , CM000678.2:g.9763617C>T	GRCh38
NC_000016.9:g.9857474C>T , CM000678.1:g.9857474C>T	GRCh37
NC_000016.8:g.9764975C>T	NCBI36
NG_011812.1:g.424138G>A
NG_011812.2:g.424138G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.3927G>A MANE Select	ENSP00000332549.3:p.Arg1309=
ENST00000535259.6:c.3301+155G>A	ENSP00000441572.3:n.3301+155G>A
ENST00000636273.2:n.3365+155G>A
ENST00000674742.1:c.3456G>A	ENSP00000502200.1:p.Arg1152=
ENST00000675398.1:c.*1297G>A	ENSP00000502752.1:n.*1297G>A
ENST00000330684.3:c.3927G>A	ENSP00000332549.3:p.Arg1309=
ENST00000396573.6:c.3927G>A	ENSP00000379818.2:p.Arg1309=
ENST00000396575.6:c.3516G>A	ENSP00000379820.3:p.Arg1172=
ENST00000461292.3:n.3411+155G>A
ENST00000535259.5:c.3361+155G>A	ENSP00000441572.2:n.3361+155G>A
ENST00000562109.5:c.3772+155G>A	ENSP00000454998.1:n.3772+155G>A
NM_000833.4:c.3927G>A	NP_000824.1:p.Arg1309=
NM_001134407.2:c.3927G>A	NP_001127879.1:p.Arg1309=
NM_001134408.2:c.3772+155G>A	NP_001127880.1:n.3772+155G>A
XM_011522456.1:c.3768G>A	XP_011520758.1:p.Arg1256=
XM_011522457.1:c.3669G>A	XP_011520759.1:p.Arg1223=
XM_011522458.1:c.3456G>A	XP_011520760.1:p.Arg1152=
XM_011522459.1:c.3456G>A	XP_011520761.1:p.Arg1152=
XM_011522460.1:c.3456G>A	XP_011520762.1:p.Arg1152=
XM_011522461.1:c.3772+155G>A	XP_011520763.1:n.3772+155G>A
XM_011522458.3:c.3456G>A	XP_011520760.1:p.Arg1152=
XM_011522461.3:c.3772+155G>A	XP_011520763.1:n.3772+155G>A
XM_017023172.1:c.4083G>A	XP_016878661.1:p.Arg1361=
XM_017023173.1:c.3928+155G>A	XP_016878662.1:n.3928+155G>A
NM_001134407.3:c.3927G>A MANE Select	NP_001127879.1:p.Arg1309=
NM_000833.5:c.3927G>A	NP_000824.1:p.Arg1309=