Canonical Allele Identifier: CA152999

Gene: GRIA3

Linked Data

• ClinVar Variation Id: 129166
• ClinVar RCV Id: RCV000117155 ; RCV000882979 ; RCV002313886
• dbSNP Id: rs61740996
• ExAC: X:122318402 G / A
• gnomAD v2: X-122318402-G-A
• gnomAD v3: X-123184550-G-A
• gnomAD v4: X-123184550-G-A
• MyVariant Identifiers: chrX:g.122318402G>A (hg19) ; chrX:g.123184550G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123184550G>A , CM000685.2:g.123184550G>A	GRCh38
NC_000023.10:g.122318402G>A , CM000685.1:g.122318402G>A	GRCh37
NC_000023.9:g.122146083G>A	NCBI36
NG_009377.2:g.5308G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.15G>A MANE Select	ENSP00000478489.1:p.Lys5=
ENST00000622768.5:c.15G>A MANE Plus Clinical	ENSP00000481554.1:p.Lys5=
ENST00000541091.5:c.15G>A	ENSP00000446440.2:p.Lys5=
ENST00000611689.4:c.15G>A	ENSP00000478758.1:p.Lys5=
ENST00000616590.4:c.15G>A	ENSP00000479607.1:p.Lys5=
ENST00000620443.1:c.15G>A	ENSP00000478489.1:p.Lys5=
ENST00000620581.4:c.15G>A	ENSP00000481875.1:p.Lys5=
ENST00000622768.4:c.15G>A	ENSP00000481554.1:p.Lys5=
NM_000828.4:c.15G>A	NP_000819.3:p.Lys5=
NM_001256743.1:c.15G>A	NP_001243672.1:p.Lys5=
NM_007325.4:c.15G>A	NP_015564.4:p.Lys5=
NM_001256743.2:c.15G>A	NP_001243672.1:p.Lys5=
NM_007325.5:c.15G>A MANE Select	NP_015564.5:p.Lys5=
NM_000828.5:c.15G>A MANE Plus Clinical	NP_000819.4:p.Lys5=