Canonical Allele Identifier: CA1868339465
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1827942100

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585665_101585666dup , CM000671.2:g.101585665_101585666dup GRCh38
NC_000009.11:g.104347947_104347948dup , CM000671.1:g.104347947_104347948dup GRCh37
NC_000009.10:g.103387768_103387769dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2767-6306_2767-6305dup MANE Select ENSP00000355155.3:n.2767-6306_2767-6305dup
ENST00000361820.3:c.2767-6306_2767-6305dup ENSP00000355155.3:n.2767-6306_2767-6305dup
NM_133445.2:c.2767-6306_2767-6305dup NP_597702.2:n.2767-6306_2767-6305dup
NM_133445.3:c.2767-6306_2767-6305dup MANE Select NP_597702.2:n.2767-6306_2767-6305dup