Canonical Allele Identifier: CA1868369275
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1828434986
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615562_101615603del , CM000671.2:g.101615562_101615603del GRCh38
NC_000009.11:g.104377844_104377885del , CM000671.1:g.104377844_104377885del GRCh37
NC_000009.10:g.103417665_103417706del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2615-2076_2615-2035del MANE Select ENSP00000355155.3:n.2615-2076_2615-2035del
ENST00000361820.3:c.2615-2076_2615-2035del ENSP00000355155.3:n.2615-2076_2615-2035del
NM_133445.2:c.2615-2076_2615-2035del NP_597702.2:n.2615-2076_2615-2035del
XM_011518211.1:c.2615-2076_2615-2035del XP_011516513.1:n.2615-2076_2615-2035del
XM_011518212.1:c.2615-2076_2615-2035del XP_011516514.1:n.2615-2076_2615-2035del
XR_929711.1:n.2702-2076_2702-2035del
XM_011518211.2:c.2615-2076_2615-2035del XP_011516513.1:n.2615-2076_2615-2035del
NM_133445.3:c.2615-2076_2615-2035del MANE Select NP_597702.2:n.2615-2076_2615-2035del
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