Canonical Allele Identifier: CA1868369279
Gene: GRIN3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615570_101615571delinsTG , CM000671.2:g.101615570_101615571delinsTG GRCh38
NC_000009.11:g.104377852_104377853delinsTG , CM000671.1:g.104377852_104377853delinsTG GRCh37
NC_000009.10:g.103417673_103417674delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2615-2044_2615-2043delinsCA MANE Select ENSP00000355155.3:n.2615-2044_2615-2043delinsCA
ENST00000361820.3:c.2615-2044_2615-2043delinsCA ENSP00000355155.3:n.2615-2044_2615-2043delinsCA
NM_133445.2:c.2615-2044_2615-2043delinsCA NP_597702.2:n.2615-2044_2615-2043delinsCA
XM_011518211.1:c.2615-2044_2615-2043delinsCA XP_011516513.1:n.2615-2044_2615-2043delinsCA
XM_011518212.1:c.2615-2044_2615-2043delinsCA XP_011516514.1:n.2615-2044_2615-2043delinsCA
XR_929711.1:n.2702-2044_2702-2043delinsCA
XM_011518211.2:c.2615-2044_2615-2043delinsCA XP_011516513.1:n.2615-2044_2615-2043delinsCA
NM_133445.3:c.2615-2044_2615-2043delinsCA MANE Select NP_597702.2:n.2615-2044_2615-2043delinsCA