Canonical Allele Identifier: CA1868369402
Gene: GRIN3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615647_101615648delinsGC , CM000671.2:g.101615647_101615648delinsGC GRCh38
NC_000009.11:g.104377929_104377930delinsGC , CM000671.1:g.104377929_104377930delinsGC GRCh37
NC_000009.10:g.103417750_103417751delinsGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2615-2121_2615-2120delinsGC MANE Select ENSP00000355155.3:n.2615-2121_2615-2120delinsGC
ENST00000361820.3:c.2615-2121_2615-2120delinsGC ENSP00000355155.3:n.2615-2121_2615-2120delinsGC
NM_133445.2:c.2615-2121_2615-2120delinsGC NP_597702.2:n.2615-2121_2615-2120delinsGC
XM_011518211.1:c.2615-2121_2615-2120delinsGC XP_011516513.1:n.2615-2121_2615-2120delinsGC
XM_011518212.1:c.2615-2121_2615-2120delinsGC XP_011516514.1:n.2615-2121_2615-2120delinsGC
XR_929711.1:n.2702-2121_2702-2120delinsGC
XM_011518211.2:c.2615-2121_2615-2120delinsGC XP_011516513.1:n.2615-2121_2615-2120delinsGC
NM_133445.3:c.2615-2121_2615-2120delinsGC MANE Select NP_597702.2:n.2615-2121_2615-2120delinsGC