Canonical Allele Identifier: CA2785331039
Gene: GRIN3A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615723G>T , CM000671.2:g.101615723G>T GRCh38
NC_000009.11:g.104378005G>T , CM000671.1:g.104378005G>T GRCh37
NC_000009.10:g.103417826G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2615-2196C>A MANE Select ENSP00000355155.3:n.2615-2196C>A
ENST00000361820.3:c.2615-2196C>A ENSP00000355155.3:n.2615-2196C>A
NM_133445.2:c.2615-2196C>A NP_597702.2:n.2615-2196C>A
XM_011518211.1:c.2615-2196C>A XP_011516513.1:n.2615-2196C>A
XM_011518212.1:c.2615-2196C>A XP_011516514.1:n.2615-2196C>A
XR_929711.1:n.2702-2196C>A
XM_011518211.2:c.2615-2196C>A XP_011516513.1:n.2615-2196C>A
NM_133445.3:c.2615-2196C>A MANE Select NP_597702.2:n.2615-2196C>A
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