Canonical Allele Identifier: CA414264712
Gene: GRIA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.123464907A>G , CM000685.2:g.123464907A>G GRCh38
NC_000023.10:g.122598758A>G , CM000685.1:g.122598758A>G GRCh37
NC_000023.9:g.122426439A>G NCBI36
NG_009377.2:g.285665A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000620443.2:c.2119A>G MANE Select ENSP00000478489.1:p.Lys707Glu
ENST00000622768.5:c.2119A>G MANE Plus Clinical ENSP00000481554.1:p.Lys707Glu
ENST00000541091.5:c.2119A>G ENSP00000446440.2:p.Lys707Glu
ENST00000620443.1:c.2119A>G ENSP00000478489.1:p.Lys707Glu
ENST00000620581.4:c.2119A>G ENSP00000481875.1:p.Lys707Glu
ENST00000622768.4:c.2119A>G ENSP00000481554.1:p.Lys707Glu
NM_000828.4:c.2119A>G NP_000819.3:p.Lys707Glu
NM_007325.4:c.2119A>G NP_015564.4:p.Lys707Glu
XR_938574.1:n.4959+1847T>C
NM_007325.5:c.2119A>G MANE Select NP_015564.5:p.Lys707Glu
NM_000828.5:c.2119A>G MANE Plus Clinical NP_000819.4:p.Lys707Glu