Canonical Allele Identifier: CA1868369462
Gene: GRIN3A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615713G= , CM000671.2:g.101615713G= GRCh38
NC_000009.11:g.104377995G= , CM000671.1:g.104377995G= GRCh37
NC_000009.10:g.103417816G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2615-2186C= MANE Select ENSP00000355155.3:n.2615-2186C=
ENST00000361820.3:c.2615-2186C= ENSP00000355155.3:n.2615-2186C=
NM_133445.2:c.2615-2186C= NP_597702.2:n.2615-2186C=
XM_011518211.1:c.2615-2186C= XP_011516513.1:n.2615-2186C=
XM_011518212.1:c.2615-2186C= XP_011516514.1:n.2615-2186C=
XR_929711.1:n.2702-2186C=
XM_011518211.2:c.2615-2186C= XP_011516513.1:n.2615-2186C=
NM_133445.3:c.2615-2186C= MANE Select NP_597702.2:n.2615-2186C=
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