Canonical Allele Identifier: CA414264752
Gene: GRIA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.123464914C>A , CM000685.2:g.123464914C>A GRCh38
NC_000023.10:g.122598765C>A , CM000685.1:g.122598765C>A GRCh37
NC_000023.9:g.122426446C>A NCBI36
NG_009377.2:g.285672C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000620443.2:c.2126C>A MANE Select ENSP00000478489.1:p.Ala709Glu
ENST00000622768.5:c.2126C>A MANE Plus Clinical ENSP00000481554.1:p.Ala709Glu
ENST00000541091.5:c.2126C>A ENSP00000446440.2:p.Ala709Glu
ENST00000620443.1:c.2126C>A ENSP00000478489.1:p.Ala709Glu
ENST00000620581.4:c.2126C>A ENSP00000481875.1:p.Ala709Glu
ENST00000622768.4:c.2126C>A ENSP00000481554.1:p.Ala709Glu
NM_000828.4:c.2126C>A NP_000819.3:p.Ala709Glu
NM_007325.4:c.2126C>A NP_015564.4:p.Ala709Glu
XR_938574.1:n.4959+1840G>T
NM_007325.5:c.2126C>A MANE Select NP_015564.5:p.Ala709Glu
NM_000828.5:c.2126C>A MANE Plus Clinical NP_000819.4:p.Ala709Glu