Canonical Allele Identifier: CA374271283

Gene: GRIN3A

Linked Data

• dbSNP Id: rs1049357004
• MyVariant Identifiers: chr9:g.104449007G>A (hg19) ; chr9:g.101686725G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101686725G>A , CM000671.2:g.101686725G>A	GRCh38
NC_000009.11:g.104449007G>A , CM000671.1:g.104449007G>A	GRCh37
NC_000009.10:g.103488828G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361820.6:c.1175C>T MANE Select	ENSP00000355155.3:p.Ala392Val
ENST00000361820.3:c.1175C>T	ENSP00000355155.3:p.Ala392Val
NM_133445.2:c.1175C>T	NP_597702.2:p.Ala392Val
XM_011518211.1:c.1175C>T	XP_011516513.1:p.Ala392Val
XM_011518212.1:c.1175C>T	XP_011516514.1:p.Ala392Val
XR_929711.1:n.1262C>T
XM_011518211.2:c.1175C>T	XP_011516513.1:p.Ala392Val
NM_133445.3:c.1175C>T MANE Select	NP_597702.2:p.Ala392Val