Canonical Allele Identifier: CA1868369497
Gene: GRIN3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615752G= , CM000671.2:g.101615752G= GRCh38
NC_000009.11:g.104378034G= , CM000671.1:g.104378034G= GRCh37
NC_000009.10:g.103417855G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2615-2225C= MANE Select ENSP00000355155.3:n.2615-2225C=
ENST00000361820.3:c.2615-2225C= ENSP00000355155.3:n.2615-2225C=
NM_133445.2:c.2615-2225C= NP_597702.2:n.2615-2225C=
XM_011518211.1:c.2615-2225C= XP_011516513.1:n.2615-2225C=
XM_011518212.1:c.2615-2225C= XP_011516514.1:n.2615-2225C=
XR_929711.1:n.2702-2225C=
XM_011518211.2:c.2615-2225C= XP_011516513.1:n.2615-2225C=
NM_133445.3:c.2615-2225C= MANE Select NP_597702.2:n.2615-2225C=