Canonical Allele Identifier: CA7896884
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 532713
dbSNP Id: rs568484876
gnomAD v3: 16-9938083-C-T
gnomAD v4: 16-9938083-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9938083C>T , CM000678.2:g.9938083C>T GRCh38
NC_000016.9:g.10031940C>T , CM000678.1:g.10031940C>T GRCh37
NC_000016.8:g.9939441C>T NCBI36
NG_011812.1:g.249672G>A
NG_011812.2:g.249672G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.883G>A MANE Select ENSP00000332549.3:p.Gly295Ser
ENST00000535259.6:c.412G>A ENSP00000441572.3:p.Gly138Ser
ENST00000636273.2:n.476G>A
ENST00000637393.1:c.475G>A ENSP00000490232.1:p.Gly159Ser
ENST00000674742.1:c.412G>A ENSP00000502200.1:p.Gly138Ser
ENST00000675189.1:n.1367G>A
ENST00000675398.1:c.883G>A ENSP00000502752.1:p.Gly295Ser
ENST00000330684.3:c.883G>A ENSP00000332549.3:p.Gly295Ser
ENST00000396573.6:c.883G>A ENSP00000379818.2:p.Gly295Ser
ENST00000396575.6:c.472G>A ENSP00000379820.3:p.Gly158Ser
ENST00000461292.3:n.522G>A
ENST00000535259.5:c.472G>A ENSP00000441572.2:p.Gly158Ser
ENST00000562109.5:c.883G>A ENSP00000454998.1:p.Gly295Ser
ENST00000566683.1:n.241-46983G>A
ENST00000568247.3:n.775G>A
NM_000833.4:c.883G>A NP_000824.1:p.Gly295Ser
NM_001134407.2:c.883G>A NP_001127879.1:p.Gly295Ser
NM_001134408.2:c.883G>A NP_001127880.1:p.Gly295Ser
XM_011522456.1:c.724G>A XP_011520758.1:p.Gly242Ser
XM_011522457.1:c.625G>A XP_011520759.1:p.Gly209Ser
XM_011522458.1:c.412G>A XP_011520760.1:p.Gly138Ser
XM_011522459.1:c.412G>A XP_011520761.1:p.Gly138Ser
XM_011522460.1:c.412G>A XP_011520762.1:p.Gly138Ser
XM_011522461.1:c.883G>A XP_011520763.1:p.Gly295Ser
XM_011522458.3:c.412G>A XP_011520760.1:p.Gly138Ser
XM_011522461.3:c.883G>A XP_011520763.1:p.Gly295Ser
XM_017023172.1:c.1039G>A XP_016878661.1:p.Gly347Ser
XM_017023173.1:c.1039G>A XP_016878662.1:p.Gly347Ser
NM_001134407.3:c.883G>A MANE Select NP_001127879.1:p.Gly295Ser
NM_000833.5:c.883G>A NP_000824.1:p.Gly295Ser