Canonical Allele Identifier: CA1868369669
Gene: GRIN3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615848_101615849delinsGA , CM000671.2:g.101615848_101615849delinsGA GRCh38
NC_000009.11:g.104378130_104378131delinsGA , CM000671.1:g.104378130_104378131delinsGA GRCh37
NC_000009.10:g.103417951_103417952delinsGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2615-2322_2615-2321delinsTC MANE Select ENSP00000355155.3:n.2615-2322_2615-2321delinsTC
ENST00000361820.3:c.2615-2322_2615-2321delinsTC ENSP00000355155.3:n.2615-2322_2615-2321delinsTC
NM_133445.2:c.2615-2322_2615-2321delinsTC NP_597702.2:n.2615-2322_2615-2321delinsTC
XM_011518211.1:c.2615-2322_2615-2321delinsTC XP_011516513.1:n.2615-2322_2615-2321delinsTC
XM_011518212.1:c.2615-2322_2615-2321delinsTC XP_011516514.1:n.2615-2322_2615-2321delinsTC
XR_929711.1:n.2702-2322_2702-2321delinsTC
XM_011518211.2:c.2615-2322_2615-2321delinsTC XP_011516513.1:n.2615-2322_2615-2321delinsTC
NM_133445.3:c.2615-2322_2615-2321delinsTC MANE Select NP_597702.2:n.2615-2322_2615-2321delinsTC