Canonical Allele Identifier: CA414260341

Gene: GRIA3

Linked Data

• gnomAD v4: X-123428137-A-G
• MyVariant Identifiers: chrX:g.122561988A>G (hg19) ; chrX:g.123428137A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123428137A>G , CM000685.2:g.123428137A>G	GRCh38
NC_000023.10:g.122561988A>G , CM000685.1:g.122561988A>G	GRCh37
NC_000023.9:g.122389669A>G	NCBI36
NG_009377.2:g.248895A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.2074A>G MANE Select	ENSP00000478489.1:p.Arg692Gly
ENST00000622768.5:c.2074A>G MANE Plus Clinical	ENSP00000481554.1:p.Arg692Gly
ENST00000541091.5:c.2074A>G	ENSP00000446440.2:p.Arg692Gly
ENST00000620443.1:c.2074A>G	ENSP00000478489.1:p.Arg692Gly
ENST00000620581.4:c.2074A>G	ENSP00000481875.1:p.Arg692Gly
ENST00000622768.4:c.2074A>G	ENSP00000481554.1:p.Arg692Gly
NM_000828.4:c.2074A>G	NP_000819.3:p.Arg692Gly
NM_007325.4:c.2074A>G	NP_015564.4:p.Arg692Gly
XR_938574.1:n.5217+9113T>C
NM_007325.5:c.2074A>G MANE Select	NP_015564.5:p.Arg692Gly
NM_000828.5:c.2074A>G MANE Plus Clinical	NP_000819.4:p.Arg692Gly