Canonical Allele Identifier: CA128602
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 29733
ClinVar RCV Id: RCV000022585
dbSNP Id: rs397518447
MyVariant Identifiers: chr16:g.9923442G>T (hg19) chr16:g.9829585G>T (hg38)
PubMed: PMID:20890276 PMID:26648591 PMID:27683935
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9829585G>T , CM000678.2:g.9829585G>T GRCh38
NC_000016.9:g.9923442G>T , CM000678.1:g.9923442G>T GRCh37
NC_000016.8:g.9830943G>T NCBI36
NG_011812.1:g.358170C>A
NG_011812.2:g.358170C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000330684.4:c.1845C>A MANE Select ENSP00000332549.3:p.Asn615Lys
ENST00000535259.6:c.1374C>A ENSP00000441572.3:p.Asn458Lys
ENST00000636273.2:n.1438C>A
ENST00000674742.1:c.1374C>A ENSP00000502200.1:p.Asn458Lys
ENST00000675398.1:c.1845C>A ENSP00000502752.1:p.Asn615Lys
ENST00000330684.3:c.1845C>A ENSP00000332549.3:p.Asn615Lys
ENST00000396573.6:c.1845C>A ENSP00000379818.2:p.Asn615Lys
ENST00000396575.6:c.1434C>A ENSP00000379820.3:p.Asn478Lys
ENST00000461292.3:n.1484C>A
ENST00000535259.5:c.1434C>A ENSP00000441572.2:p.Asn478Lys
ENST00000562109.5:c.1845C>A ENSP00000454998.1:p.Asn615Lys
NM_000833.4:c.1845C>A NP_000824.1:p.Asn615Lys
NM_001134407.2:c.1845C>A NP_001127879.1:p.Asn615Lys
NM_001134408.2:c.1845C>A NP_001127880.1:p.Asn615Lys
XM_011522456.1:c.1686C>A XP_011520758.1:p.Asn562Lys
XM_011522457.1:c.1587C>A XP_011520759.1:p.Asn529Lys
XM_011522458.1:c.1374C>A XP_011520760.1:p.Asn458Lys
XM_011522459.1:c.1374C>A XP_011520761.1:p.Asn458Lys
XM_011522460.1:c.1374C>A XP_011520762.1:p.Asn458Lys
XM_011522461.1:c.1845C>A XP_011520763.1:p.Asn615Lys
XM_011522458.3:c.1374C>A XP_011520760.1:p.Asn458Lys
XM_011522461.3:c.1845C>A XP_011520763.1:p.Asn615Lys
XM_017023172.1:c.2001C>A XP_016878661.1:p.Asn667Lys
XM_017023173.1:c.2001C>A XP_016878662.1:p.Asn667Lys
NM_001134407.3:c.1845C>A MANE Select NP_001127879.1:p.Asn615Lys
NM_000833.5:c.1845C>A NP_000824.1:p.Asn615Lys
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