Canonical Allele Identifier: CA466470749

Gene: GRIN3A

Linked Data

• MyVariant Identifiers: chr9:g.104448999G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101686717G>A , CM000671.2:g.101686717G>A	GRCh38
NC_000009.11:g.104448999G>A , CM000671.1:g.104448999G>A	GRCh37
NC_000009.10:g.103488820G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361820.6:c.1183C>T MANE Select	ENSP00000355155.3:p.Leu395=
ENST00000361820.3:c.1183C>T	ENSP00000355155.3:p.Leu395=
NM_133445.2:c.1183C>T	NP_597702.2:p.Leu395=
XM_011518211.1:c.1183C>T	XP_011516513.1:p.Leu395=
XM_011518212.1:c.1183C>T	XP_011516514.1:p.Leu395=
XR_929711.1:n.1270C>T
XM_011518211.2:c.1183C>T	XP_011516513.1:p.Leu395=
NM_133445.3:c.1183C>T MANE Select	NP_597702.2:p.Leu395=