Canonical Allele Identifier: CA394798134
Gene: GRIN2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9938008A>C , CM000678.2:g.9938008A>C GRCh38
NC_000016.9:g.10031865A>C , CM000678.1:g.10031865A>C GRCh37
NC_000016.8:g.9939366A>C NCBI36
NG_011812.1:g.249747T>G
NG_011812.2:g.249747T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.958T>G MANE Select ENSP00000332549.3:p.Cys320Gly
ENST00000535259.6:c.487T>G ENSP00000441572.3:p.Cys163Gly
ENST00000636273.2:n.551T>G
ENST00000637393.1:c.550T>G ENSP00000490232.1:p.Cys184Gly
ENST00000674742.1:c.487T>G ENSP00000502200.1:p.Cys163Gly
ENST00000675189.1:n.1442T>G
ENST00000675398.1:c.958T>G ENSP00000502752.1:p.Cys320Gly
ENST00000330684.3:c.958T>G ENSP00000332549.3:p.Cys320Gly
ENST00000396573.6:c.958T>G ENSP00000379818.2:p.Cys320Gly
ENST00000396575.6:c.547T>G ENSP00000379820.3:p.Cys183Gly
ENST00000461292.3:n.597T>G
ENST00000535259.5:c.547T>G ENSP00000441572.2:p.Cys183Gly
ENST00000562109.5:c.958T>G ENSP00000454998.1:p.Cys320Gly
ENST00000566683.1:n.241-46908T>G
ENST00000568247.3:n.850T>G
NM_000833.4:c.958T>G NP_000824.1:p.Cys320Gly
NM_001134407.2:c.958T>G NP_001127879.1:p.Cys320Gly
NM_001134408.2:c.958T>G NP_001127880.1:p.Cys320Gly
XM_011522456.1:c.799T>G XP_011520758.1:p.Cys267Gly
XM_011522457.1:c.700T>G XP_011520759.1:p.Cys234Gly
XM_011522458.1:c.487T>G XP_011520760.1:p.Cys163Gly
XM_011522459.1:c.487T>G XP_011520761.1:p.Cys163Gly
XM_011522460.1:c.487T>G XP_011520762.1:p.Cys163Gly
XM_011522461.1:c.958T>G XP_011520763.1:p.Cys320Gly
XM_011522458.3:c.487T>G XP_011520760.1:p.Cys163Gly
XM_011522461.3:c.958T>G XP_011520763.1:p.Cys320Gly
XM_017023172.1:c.1114T>G XP_016878661.1:p.Cys372Gly
XM_017023173.1:c.1114T>G XP_016878662.1:p.Cys372Gly
NM_001134407.3:c.958T>G MANE Select NP_001127879.1:p.Cys320Gly
NM_000833.5:c.958T>G NP_000824.1:p.Cys320Gly