Canonical Allele Identifier: CA414264475

Gene: GRIA3

Linked Data

• MyVariant Identifiers: chrX:g.122598720C>A (hg19) ; chrX:g.123464869C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123464869C>A , CM000685.2:g.123464869C>A	GRCh38
NC_000023.10:g.122598720C>A , CM000685.1:g.122598720C>A	GRCh37
NC_000023.9:g.122426401C>A	NCBI36
NG_009377.2:g.285627C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.2081C>A MANE Select	ENSP00000478489.1:p.Ser694Tyr
ENST00000622768.5:c.2081C>A MANE Plus Clinical	ENSP00000481554.1:p.Ser694Tyr
ENST00000541091.5:c.2081C>A	ENSP00000446440.2:p.Ser694Tyr
ENST00000620443.1:c.2081C>A	ENSP00000478489.1:p.Ser694Tyr
ENST00000620581.4:c.2081C>A	ENSP00000481875.1:p.Ser694Tyr
ENST00000622768.4:c.2081C>A	ENSP00000481554.1:p.Ser694Tyr
NM_000828.4:c.2081C>A	NP_000819.3:p.Ser694Tyr
NM_007325.4:c.2081C>A	NP_015564.4:p.Ser694Tyr
XR_938574.1:n.4959+1885G>T
NM_007325.5:c.2081C>A MANE Select	NP_015564.5:p.Ser694Tyr
NM_000828.5:c.2081C>A MANE Plus Clinical	NP_000819.4:p.Ser694Tyr