Canonical Allele Identifier: CA1868339568
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1827944831

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585875del , CM000671.2:g.101585875del GRCh38
NC_000009.11:g.104348157del , CM000671.1:g.104348157del GRCh37
NC_000009.10:g.103387978del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2767-6513del MANE Select ENSP00000355155.3:n.2767-6513del
ENST00000361820.3:c.2767-6513del ENSP00000355155.3:n.2767-6513del
NM_133445.2:c.2767-6513del NP_597702.2:n.2767-6513del
NM_133445.3:c.2767-6513del MANE Select NP_597702.2:n.2767-6513del