Canonical Allele Identifier: CA2206693420
Gene: GRIN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9764794G= , CM000678.2:g.9764794G= GRCh38
NC_000016.9:g.9858651G= , CM000678.1:g.9858651G= GRCh37
NC_000016.8:g.9766152G= NCBI36
NG_011812.1:g.422961C=
NG_011812.2:g.422961C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.2750C= MANE Select ENSP00000332549.3:p.Ser917=
ENST00000535259.6:c.2279C= ENSP00000441572.3:p.Ser760=
ENST00000636273.2:n.2343C=
ENST00000674742.1:c.2279C= ENSP00000502200.1:p.Ser760=
ENST00000675398.1:c.*120C= ENSP00000502752.1:n.*120C=
ENST00000330684.3:c.2750C= ENSP00000332549.3:p.Ser917=
ENST00000396573.6:c.2750C= ENSP00000379818.2:p.Ser917=
ENST00000396575.6:c.2339C= ENSP00000379820.3:p.Ser780=
ENST00000461292.3:n.2389C=
ENST00000535259.5:c.2339C= ENSP00000441572.2:p.Ser780=
ENST00000562109.5:c.2750C= ENSP00000454998.1:p.Ser917=
NM_000833.4:c.2750C= NP_000824.1:p.Ser917=
NM_001134407.2:c.2750C= NP_001127879.1:p.Ser917=
NM_001134408.2:c.2750C= NP_001127880.1:p.Ser917=
XM_011522456.1:c.2591C= XP_011520758.1:p.Ser864=
XM_011522457.1:c.2492C= XP_011520759.1:p.Ser831=
XM_011522458.1:c.2279C= XP_011520760.1:p.Ser760=
XM_011522459.1:c.2279C= XP_011520761.1:p.Ser760=
XM_011522460.1:c.2279C= XP_011520762.1:p.Ser760=
XM_011522461.1:c.2750C= XP_011520763.1:p.Ser917=
XM_011522458.3:c.2279C= XP_011520760.1:p.Ser760=
XM_011522461.3:c.2750C= XP_011520763.1:p.Ser917=
XM_017023172.1:c.2906C= XP_016878661.1:p.Ser969=
XM_017023173.1:c.2906C= XP_016878662.1:p.Ser969=
NM_001134407.3:c.2750C= MANE Select NP_001127879.1:p.Ser917=
NM_000833.5:c.2750C= NP_000824.1:p.Ser917=