Canonical Allele Identifier: CA1868423115
Gene: GRIN3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101686723T= , CM000671.2:g.101686723T= GRCh38
NC_000009.11:g.104449005T= , CM000671.1:g.104449005T= GRCh37
NC_000009.10:g.103488826T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.1177A= MANE Select ENSP00000355155.3:p.Met393=
ENST00000361820.3:c.1177A= ENSP00000355155.3:p.Met393=
NM_133445.2:c.1177A= NP_597702.2:p.Met393=
XM_011518211.1:c.1177A= XP_011516513.1:p.Met393=
XM_011518212.1:c.1177A= XP_011516514.1:p.Met393=
XR_929711.1:n.1264A=
XM_011518211.2:c.1177A= XP_011516513.1:p.Met393=
NM_133445.3:c.1177A= MANE Select NP_597702.2:p.Met393=