Canonical Allele Identifier: CA314943
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 205654
ClinVar RCV Id: RCV000187640 RCV001781549
dbSNP Id: rs796052547
MyVariant Identifiers: chr16:g.9916239T>C (hg19) chr16:g.9822382T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9822382T>C , CM000678.2:g.9822382T>C GRCh38
NC_000016.9:g.9916239T>C , CM000678.1:g.9916239T>C GRCh37
NC_000016.8:g.9823740T>C NCBI36
NG_011812.1:g.365373A>G
NG_011812.2:g.365373A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000330684.4:c.2050A>G MANE Select ENSP00000332549.3:p.Thr684Ala
ENST00000535259.6:c.1579A>G ENSP00000441572.3:p.Thr527Ala
ENST00000636273.2:n.1643A>G
ENST00000674742.1:c.1579A>G ENSP00000502200.1:p.Thr527Ala
ENST00000675398.1:c.2050A>G ENSP00000502752.1:p.Thr684Ala
ENST00000330684.3:c.2050A>G ENSP00000332549.3:p.Thr684Ala
ENST00000396573.6:c.2050A>G ENSP00000379818.2:p.Thr684Ala
ENST00000396575.6:c.1639A>G ENSP00000379820.3:p.Thr547Ala
ENST00000461292.3:n.1689A>G
ENST00000535259.5:c.1639A>G ENSP00000441572.2:p.Thr547Ala
ENST00000562109.5:c.2050A>G ENSP00000454998.1:p.Thr684Ala
NM_000833.4:c.2050A>G NP_000824.1:p.Thr684Ala
NM_001134407.2:c.2050A>G NP_001127879.1:p.Thr684Ala
NM_001134408.2:c.2050A>G NP_001127880.1:p.Thr684Ala
XM_011522456.1:c.1891A>G XP_011520758.1:p.Thr631Ala
XM_011522457.1:c.1792A>G XP_011520759.1:p.Thr598Ala
XM_011522458.1:c.1579A>G XP_011520760.1:p.Thr527Ala
XM_011522459.1:c.1579A>G XP_011520761.1:p.Thr527Ala
XM_011522460.1:c.1579A>G XP_011520762.1:p.Thr527Ala
XM_011522461.1:c.2050A>G XP_011520763.1:p.Thr684Ala
XM_011522458.3:c.1579A>G XP_011520760.1:p.Thr527Ala
XM_011522461.3:c.2050A>G XP_011520763.1:p.Thr684Ala
XM_017023172.1:c.2206A>G XP_016878661.1:p.Thr736Ala
XM_017023173.1:c.2206A>G XP_016878662.1:p.Thr736Ala
NM_001134407.3:c.2050A>G MANE Select NP_001127879.1:p.Thr684Ala
NM_000833.5:c.2050A>G NP_000824.1:p.Thr684Ala
Search 100 bp 5'
Search 100 bp 3'