Canonical Allele Identifier: CA1868369441
Gene: GRIN3A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615694T= , CM000671.2:g.101615694T= GRCh38
NC_000009.11:g.104377976T= , CM000671.1:g.104377976T= GRCh37
NC_000009.10:g.103417797T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2615-2167A= MANE Select ENSP00000355155.3:n.2615-2167A=
ENST00000361820.3:c.2615-2167A= ENSP00000355155.3:n.2615-2167A=
NM_133445.2:c.2615-2167A= NP_597702.2:n.2615-2167A=
XM_011518211.1:c.2615-2167A= XP_011516513.1:n.2615-2167A=
XM_011518212.1:c.2615-2167A= XP_011516514.1:n.2615-2167A=
XR_929711.1:n.2702-2167A=
XM_011518211.2:c.2615-2167A= XP_011516513.1:n.2615-2167A=
NM_133445.3:c.2615-2167A= MANE Select NP_597702.2:n.2615-2167A=
Search 100 bp 5'
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