Canonical Allele Identifier: CA7896883
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2807719
ClinVar RCV Id: RCV003741670
dbSNP Id: rs775591257
gnomAD v4: 16-9938076-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9938076C>G , CM000678.2:g.9938076C>G GRCh38
NC_000016.9:g.10031933C>G , CM000678.1:g.10031933C>G GRCh37
NC_000016.8:g.9939434C>G NCBI36
NG_011812.1:g.249679G>C
NG_011812.2:g.249679G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.890G>C MANE Select ENSP00000332549.3:p.Gly297Ala
ENST00000535259.6:c.419G>C ENSP00000441572.3:p.Gly140Ala
ENST00000636273.2:n.483G>C
ENST00000637393.1:c.482G>C ENSP00000490232.1:p.Gly161Ala
ENST00000674742.1:c.419G>C ENSP00000502200.1:p.Gly140Ala
ENST00000675189.1:n.1374G>C
ENST00000675398.1:c.890G>C ENSP00000502752.1:p.Gly297Ala
ENST00000330684.3:c.890G>C ENSP00000332549.3:p.Gly297Ala
ENST00000396573.6:c.890G>C ENSP00000379818.2:p.Gly297Ala
ENST00000396575.6:c.479G>C ENSP00000379820.3:p.Gly160Ala
ENST00000461292.3:n.529G>C
ENST00000535259.5:c.479G>C ENSP00000441572.2:p.Gly160Ala
ENST00000562109.5:c.890G>C ENSP00000454998.1:p.Gly297Ala
ENST00000566683.1:n.241-46976G>C
ENST00000568247.3:n.782G>C
NM_000833.4:c.890G>C NP_000824.1:p.Gly297Ala
NM_001134407.2:c.890G>C NP_001127879.1:p.Gly297Ala
NM_001134408.2:c.890G>C NP_001127880.1:p.Gly297Ala
XM_011522456.1:c.731G>C XP_011520758.1:p.Gly244Ala
XM_011522457.1:c.632G>C XP_011520759.1:p.Gly211Ala
XM_011522458.1:c.419G>C XP_011520760.1:p.Gly140Ala
XM_011522459.1:c.419G>C XP_011520761.1:p.Gly140Ala
XM_011522460.1:c.419G>C XP_011520762.1:p.Gly140Ala
XM_011522461.1:c.890G>C XP_011520763.1:p.Gly297Ala
XM_011522458.3:c.419G>C XP_011520760.1:p.Gly140Ala
XM_011522461.3:c.890G>C XP_011520763.1:p.Gly297Ala
XM_017023172.1:c.1046G>C XP_016878661.1:p.Gly349Ala
XM_017023173.1:c.1046G>C XP_016878662.1:p.Gly349Ala
NM_001134407.3:c.890G>C MANE Select NP_001127879.1:p.Gly297Ala
NM_000833.5:c.890G>C NP_000824.1:p.Gly297Ala