Canonical Allele Identifier: CA1868423125
Gene: GRIN3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101686726C= , CM000671.2:g.101686726C= GRCh38
NC_000009.11:g.104449008C= , CM000671.1:g.104449008C= GRCh37
NC_000009.10:g.103488829C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.1174G= MANE Select ENSP00000355155.3:p.Ala392=
ENST00000361820.3:c.1174G= ENSP00000355155.3:p.Ala392=
NM_133445.2:c.1174G= NP_597702.2:p.Ala392=
XM_011518211.1:c.1174G= XP_011516513.1:p.Ala392=
XM_011518212.1:c.1174G= XP_011516514.1:p.Ala392=
XR_929711.1:n.1261G=
XM_011518211.2:c.1174G= XP_011516513.1:p.Ala392=
NM_133445.3:c.1174G= MANE Select NP_597702.2:p.Ala392=