Canonical Allele Identifier: CA493702304
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1151282
ClinVar RCV Id: RCV001492136
dbSNP Id: rs2141631974
MyVariant Identifiers: chr16:g.10032214C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9938357C>T , CM000678.2:g.9938357C>T GRCh38
NC_000016.9:g.10032214C>T , CM000678.1:g.10032214C>T GRCh37
NC_000016.8:g.9939715C>T NCBI36
NG_011812.1:g.249398G>A
NG_011812.2:g.249398G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.609G>A MANE Select ENSP00000332549.3:p.Val203=
ENST00000535259.6:c.138G>A ENSP00000441572.3:p.Val46=
ENST00000636273.2:n.202G>A
ENST00000637393.1:c.201G>A ENSP00000490232.1:p.Val67=
ENST00000674742.1:c.138G>A ENSP00000502200.1:p.Val46=
ENST00000675189.1:n.1093G>A
ENST00000675398.1:c.609G>A ENSP00000502752.1:p.Val203=
ENST00000330684.3:c.609G>A ENSP00000332549.3:p.Val203=
ENST00000396573.6:c.609G>A ENSP00000379818.2:p.Val203=
ENST00000396575.6:c.198G>A ENSP00000379820.3:p.Val66=
ENST00000461292.3:n.248G>A
ENST00000535259.5:c.198G>A ENSP00000441572.2:p.Val66=
ENST00000562109.5:c.609G>A ENSP00000454998.1:p.Val203=
ENST00000566670.2:n.451G>A
ENST00000566683.1:n.241-47257G>A
ENST00000568247.3:n.501G>A
NM_000833.4:c.609G>A NP_000824.1:p.Val203=
NM_001134407.2:c.609G>A NP_001127879.1:p.Val203=
NM_001134408.2:c.609G>A NP_001127880.1:p.Val203=
XM_011522456.1:c.450G>A XP_011520758.1:p.Val150=
XM_011522457.1:c.351G>A XP_011520759.1:p.Val117=
XM_011522458.1:c.138G>A XP_011520760.1:p.Val46=
XM_011522459.1:c.138G>A XP_011520761.1:p.Val46=
XM_011522460.1:c.138G>A XP_011520762.1:p.Val46=
XM_011522461.1:c.609G>A XP_011520763.1:p.Val203=
XM_011522458.3:c.138G>A XP_011520760.1:p.Val46=
XM_011522461.3:c.609G>A XP_011520763.1:p.Val203=
XM_017023172.1:c.765G>A XP_016878661.1:p.Val255=
XM_017023173.1:c.765G>A XP_016878662.1:p.Val255=
NM_001134407.3:c.609G>A MANE Select NP_001127879.1:p.Val203=
NM_000833.5:c.609G>A NP_000824.1:p.Val203=