Canonical Allele Identifier: CA1868423130
Gene: GRIN3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101686727A= , CM000671.2:g.101686727A= GRCh38
NC_000009.11:g.104449009A= , CM000671.1:g.104449009A= GRCh37
NC_000009.10:g.103488830A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.1173T= MANE Select ENSP00000355155.3:p.Asp391=
ENST00000361820.3:c.1173T= ENSP00000355155.3:p.Asp391=
NM_133445.2:c.1173T= NP_597702.2:p.Asp391=
XM_011518211.1:c.1173T= XP_011516513.1:p.Asp391=
XM_011518212.1:c.1173T= XP_011516514.1:p.Asp391=
XR_929711.1:n.1260T=
XM_011518211.2:c.1173T= XP_011516513.1:p.Asp391=
NM_133445.3:c.1173T= MANE Select NP_597702.2:p.Asp391=