Canonical Allele Identifier: CA414264454
Gene: GRIA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.123464866G>A , CM000685.2:g.123464866G>A GRCh38
NC_000023.10:g.122598717G>A , CM000685.1:g.122598717G>A GRCh37
NC_000023.9:g.122426398G>A NCBI36
NG_009377.2:g.285624G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000620443.2:c.2078G>A MANE Select ENSP00000478489.1:p.Arg693Lys
ENST00000622768.5:c.2078G>A MANE Plus Clinical ENSP00000481554.1:p.Arg693Lys
ENST00000541091.5:c.2078G>A ENSP00000446440.2:p.Arg693Lys
ENST00000620443.1:c.2078G>A ENSP00000478489.1:p.Arg693Lys
ENST00000620581.4:c.2078G>A ENSP00000481875.1:p.Arg693Lys
ENST00000622768.4:c.2078G>A ENSP00000481554.1:p.Arg693Lys
NM_000828.4:c.2078G>A NP_000819.3:p.Arg693Lys
NM_007325.4:c.2078G>A NP_015564.4:p.Arg693Lys
XR_938574.1:n.4959+1888C>T
NM_007325.5:c.2078G>A MANE Select NP_015564.5:p.Arg693Lys
NM_000828.5:c.2078G>A MANE Plus Clinical NP_000819.4:p.Arg693Lys