Canonical Allele Identifier: CA1868339489
Gene: GRIN3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585710A= , CM000671.2:g.101585710A= GRCh38
NC_000009.11:g.104347992A= , CM000671.1:g.104347992A= GRCh37
NC_000009.10:g.103387813A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2767-6350T= MANE Select ENSP00000355155.3:n.2767-6350T=
ENST00000361820.3:c.2767-6350T= ENSP00000355155.3:n.2767-6350T=
NM_133445.2:c.2767-6350T= NP_597702.2:n.2767-6350T=
NM_133445.3:c.2767-6350T= MANE Select NP_597702.2:n.2767-6350T=