Canonical Allele Identifier: CA10507140

Gene: GRIA3

Linked Data

• dbSNP Id: rs760032706
• ExAC: X:122598702 T / C
• gnomAD v2: X-122598702-T-C
• gnomAD v4: X-123464851-T-C
• MyVariant Identifiers: chrX:g.122598702T>C (hg19) ; chrX:g.123464851T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123464851T>C , CM000685.2:g.123464851T>C	GRCh38
NC_000023.10:g.122598702T>C , CM000685.1:g.122598702T>C	GRCh37
NC_000023.9:g.122426383T>C	NCBI36
NG_009377.2:g.285609T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.2077-14T>C MANE Select	ENSP00000478489.1:n.2077-14T>C
ENST00000622768.5:c.2077-14T>C MANE Plus Clinical	ENSP00000481554.1:n.2077-14T>C
ENST00000541091.5:c.2077-14T>C	ENSP00000446440.2:n.2077-14T>C
ENST00000620443.1:c.2077-14T>C	ENSP00000478489.1:n.2077-14T>C
ENST00000620581.4:c.2077-14T>C	ENSP00000481875.1:n.2077-14T>C
ENST00000622768.4:c.2077-14T>C	ENSP00000481554.1:n.2077-14T>C
NM_000828.4:c.2077-14T>C	NP_000819.3:n.2077-14T>C
NM_007325.4:c.2077-14T>C	NP_015564.4:n.2077-14T>C
XR_938574.1:n.4959+1903A>G
NM_007325.5:c.2077-14T>C MANE Select	NP_015564.5:n.2077-14T>C
NM_000828.5:c.2077-14T>C MANE Plus Clinical	NP_000819.4:n.2077-14T>C