Canonical Allele Identifier: CA1868369267
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1828434834

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615557_101615558del , CM000671.2:g.101615557_101615558del GRCh38
NC_000009.11:g.104377839_104377840del , CM000671.1:g.104377839_104377840del GRCh37
NC_000009.10:g.103417660_103417661del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2615-2031_2615-2030del MANE Select ENSP00000355155.3:n.2615-2031_2615-2030del
ENST00000361820.3:c.2615-2031_2615-2030del ENSP00000355155.3:n.2615-2031_2615-2030del
NM_133445.2:c.2615-2031_2615-2030del NP_597702.2:n.2615-2031_2615-2030del
XM_011518211.1:c.2615-2031_2615-2030del XP_011516513.1:n.2615-2031_2615-2030del
XM_011518212.1:c.2615-2031_2615-2030del XP_011516514.1:n.2615-2031_2615-2030del
XR_929711.1:n.2702-2031_2702-2030del
XM_011518211.2:c.2615-2031_2615-2030del XP_011516513.1:n.2615-2031_2615-2030del
NM_133445.3:c.2615-2031_2615-2030del MANE Select NP_597702.2:n.2615-2031_2615-2030del