Canonical Allele Identifier: CA10507131

Gene: GRIA3

Linked Data

• dbSNP Id: rs754882028
• ExAC: X:122561963 C / T
• gnomAD v4: X-123428112-C-T
• MyVariant Identifiers: chrX:g.122561963C>T (hg19) ; chrX:g.123428112C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123428112C>T , CM000685.2:g.123428112C>T	GRCh38
NC_000023.10:g.122561963C>T , CM000685.1:g.122561963C>T	GRCh37
NC_000023.9:g.122389644C>T	NCBI36
NG_009377.2:g.248870C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.2049C>T MANE Select	ENSP00000478489.1:p.Asp683=
ENST00000622768.5:c.2049C>T MANE Plus Clinical	ENSP00000481554.1:p.Asp683=
ENST00000541091.5:c.2049C>T	ENSP00000446440.2:p.Asp683=
ENST00000620443.1:c.2049C>T	ENSP00000478489.1:p.Asp683=
ENST00000620581.4:c.2049C>T	ENSP00000481875.1:p.Asp683=
ENST00000622768.4:c.2049C>T	ENSP00000481554.1:p.Asp683=
NM_000828.4:c.2049C>T	NP_000819.3:p.Asp683=
NM_007325.4:c.2049C>T	NP_015564.4:p.Asp683=
XR_938574.1:n.5217+9138G>A
NM_007325.5:c.2049C>T MANE Select	NP_015564.5:p.Asp683=
NM_000828.5:c.2049C>T MANE Plus Clinical	NP_000819.4:p.Asp683=