Canonical Allele Identifier: CA278179182

Gene: GRIN2A

Linked Data

• ClinVar Variation Id: 1084549
• ClinVar RCV Id: RCV001401621
• dbSNP Id: rs9806806
• gnomAD v3: 16-9822347-C-T
• gnomAD v4: 16-9822347-C-T
• MyVariant Identifiers: chr16:g.9916204C>T (hg19) ; chr16:g.9822347C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9822347C>T , CM000678.2:g.9822347C>T	GRCh38
NC_000016.9:g.9916204C>T , CM000678.1:g.9916204C>T	GRCh37
NC_000016.8:g.9823705C>T	NCBI36
NG_011812.1:g.365408G>A
NG_011812.2:g.365408G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.2085G>A MANE Select	ENSP00000332549.3:p.Arg695=
ENST00000535259.6:c.1614G>A	ENSP00000441572.3:p.Arg538=
ENST00000636273.2:n.1678G>A
ENST00000674742.1:c.1614G>A	ENSP00000502200.1:p.Arg538=
ENST00000675398.1:c.2085G>A	ENSP00000502752.1:p.Arg695=
ENST00000330684.3:c.2085G>A	ENSP00000332549.3:p.Arg695=
ENST00000396573.6:c.2085G>A	ENSP00000379818.2:p.Arg695=
ENST00000396575.6:c.1674G>A	ENSP00000379820.3:p.Arg558=
ENST00000461292.3:n.1724G>A
ENST00000535259.5:c.1674G>A	ENSP00000441572.2:p.Arg558=
ENST00000562109.5:c.2085G>A	ENSP00000454998.1:p.Arg695=
NM_000833.4:c.2085G>A	NP_000824.1:p.Arg695=
NM_001134407.2:c.2085G>A	NP_001127879.1:p.Arg695=
NM_001134408.2:c.2085G>A	NP_001127880.1:p.Arg695=
XM_011522456.1:c.1926G>A	XP_011520758.1:p.Arg642=
XM_011522457.1:c.1827G>A	XP_011520759.1:p.Arg609=
XM_011522458.1:c.1614G>A	XP_011520760.1:p.Arg538=
XM_011522459.1:c.1614G>A	XP_011520761.1:p.Arg538=
XM_011522460.1:c.1614G>A	XP_011520762.1:p.Arg538=
XM_011522461.1:c.2085G>A	XP_011520763.1:p.Arg695=
XM_011522458.3:c.1614G>A	XP_011520760.1:p.Arg538=
XM_011522461.3:c.2085G>A	XP_011520763.1:p.Arg695=
XM_017023172.1:c.2241G>A	XP_016878661.1:p.Arg747=
XM_017023173.1:c.2241G>A	XP_016878662.1:p.Arg747=
NM_001134407.3:c.2085G>A MANE Select	NP_001127879.1:p.Arg695=
NM_000833.5:c.2085G>A	NP_000824.1:p.Arg695=