Canonical Allele Identifier: CA1868339538
Gene: GRIN3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585814G= , CM000671.2:g.101585814G= GRCh38
NC_000009.11:g.104348096G= , CM000671.1:g.104348096G= GRCh37
NC_000009.10:g.103387917G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2767-6454C= MANE Select ENSP00000355155.3:n.2767-6454C=
ENST00000361820.3:c.2767-6454C= ENSP00000355155.3:n.2767-6454C=
NM_133445.2:c.2767-6454C= NP_597702.2:n.2767-6454C=
NM_133445.3:c.2767-6454C= MANE Select NP_597702.2:n.2767-6454C=