Canonical Allele Identifier: CA1868369333
Gene: GRIN3A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615599C= , CM000671.2:g.101615599C= GRCh38
NC_000009.11:g.104377881C= , CM000671.1:g.104377881C= GRCh37
NC_000009.10:g.103417702C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2615-2072G= MANE Select ENSP00000355155.3:n.2615-2072G=
ENST00000361820.3:c.2615-2072G= ENSP00000355155.3:n.2615-2072G=
NM_133445.2:c.2615-2072G= NP_597702.2:n.2615-2072G=
XM_011518211.1:c.2615-2072G= XP_011516513.1:n.2615-2072G=
XM_011518212.1:c.2615-2072G= XP_011516514.1:n.2615-2072G=
XR_929711.1:n.2702-2072G=
XM_011518211.2:c.2615-2072G= XP_011516513.1:n.2615-2072G=
NM_133445.3:c.2615-2072G= MANE Select NP_597702.2:n.2615-2072G=
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