Canonical Allele Identifier: CA414259882

Gene: GRIA3

Linked Data

• gnomAD v4: X-123428036-T-A
• MyVariant Identifiers: chrX:g.122561887T>A (hg19) ; chrX:g.123428036T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123428036T>A , CM000685.2:g.123428036T>A	GRCh38
NC_000023.10:g.122561887T>A , CM000685.1:g.122561887T>A	GRCh37
NC_000023.9:g.122389568T>A	NCBI36
NG_009377.2:g.248794T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.1973T>A MANE Select	ENSP00000478489.1:p.Val658Glu
ENST00000622768.5:c.1973T>A MANE Plus Clinical	ENSP00000481554.1:p.Val658Glu
ENST00000541091.5:c.1973T>A	ENSP00000446440.2:p.Val658Glu
ENST00000620443.1:c.1973T>A	ENSP00000478489.1:p.Val658Glu
ENST00000620581.4:c.1973T>A	ENSP00000481875.1:p.Val658Glu
ENST00000622768.4:c.1973T>A	ENSP00000481554.1:p.Val658Glu
NM_000828.4:c.1973T>A	NP_000819.3:p.Val658Glu
NM_007325.4:c.1973T>A	NP_015564.4:p.Val658Glu
XR_938574.1:n.5217+9214A>T
NM_007325.5:c.1973T>A MANE Select	NP_015564.5:p.Val658Glu
NM_000828.5:c.1973T>A MANE Plus Clinical	NP_000819.4:p.Val658Glu