Canonical Allele Identifier: CA394798273
Gene: GRIN2A HGNC NCBI

Linked Data

dbSNP Id: rs1246789585
gnomAD v4: 16-9938074-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9938074T>C , CM000678.2:g.9938074T>C GRCh38
NC_000016.9:g.10031931T>C , CM000678.1:g.10031931T>C GRCh37
NC_000016.8:g.9939432T>C NCBI36
NG_011812.1:g.249681A>G
NG_011812.2:g.249681A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.892A>G MANE Select ENSP00000332549.3:p.Ile298Val
ENST00000535259.6:c.421A>G ENSP00000441572.3:p.Ile141Val
ENST00000636273.2:n.485A>G
ENST00000637393.1:c.484A>G ENSP00000490232.1:p.Ile162Val
ENST00000674742.1:c.421A>G ENSP00000502200.1:p.Ile141Val
ENST00000675189.1:n.1376A>G
ENST00000675398.1:c.892A>G ENSP00000502752.1:p.Ile298Val
ENST00000330684.3:c.892A>G ENSP00000332549.3:p.Ile298Val
ENST00000396573.6:c.892A>G ENSP00000379818.2:p.Ile298Val
ENST00000396575.6:c.481A>G ENSP00000379820.3:p.Ile161Val
ENST00000461292.3:n.531A>G
ENST00000535259.5:c.481A>G ENSP00000441572.2:p.Ile161Val
ENST00000562109.5:c.892A>G ENSP00000454998.1:p.Ile298Val
ENST00000566683.1:n.241-46974A>G
ENST00000568247.3:n.784A>G
NM_000833.4:c.892A>G NP_000824.1:p.Ile298Val
NM_001134407.2:c.892A>G NP_001127879.1:p.Ile298Val
NM_001134408.2:c.892A>G NP_001127880.1:p.Ile298Val
XM_011522456.1:c.733A>G XP_011520758.1:p.Ile245Val
XM_011522457.1:c.634A>G XP_011520759.1:p.Ile212Val
XM_011522458.1:c.421A>G XP_011520760.1:p.Ile141Val
XM_011522459.1:c.421A>G XP_011520761.1:p.Ile141Val
XM_011522460.1:c.421A>G XP_011520762.1:p.Ile141Val
XM_011522461.1:c.892A>G XP_011520763.1:p.Ile298Val
XM_011522458.3:c.421A>G XP_011520760.1:p.Ile141Val
XM_011522461.3:c.892A>G XP_011520763.1:p.Ile298Val
XM_017023172.1:c.1048A>G XP_016878661.1:p.Ile350Val
XM_017023173.1:c.1048A>G XP_016878662.1:p.Ile350Val
NM_001134407.3:c.892A>G MANE Select NP_001127879.1:p.Ile298Val
NM_000833.5:c.892A>G NP_000824.1:p.Ile298Val