Canonical Allele Identifier: CA414260341
Gene: GRIA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.123428137A>G , CM000685.2:g.123428137A>G GRCh38
NC_000023.10:g.122561988A>G , CM000685.1:g.122561988A>G GRCh37
NC_000023.9:g.122389669A>G NCBI36
NG_009377.2:g.248895A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000620443.2:c.2074A>G MANE Select ENSP00000478489.1:p.Arg692Gly
ENST00000622768.5:c.2074A>G MANE Plus Clinical ENSP00000481554.1:p.Arg692Gly
ENST00000541091.5:c.2074A>G ENSP00000446440.2:p.Arg692Gly
ENST00000620443.1:c.2074A>G ENSP00000478489.1:p.Arg692Gly
ENST00000620581.4:c.2074A>G ENSP00000481875.1:p.Arg692Gly
ENST00000622768.4:c.2074A>G ENSP00000481554.1:p.Arg692Gly
NM_000828.4:c.2074A>G NP_000819.3:p.Arg692Gly
NM_007325.4:c.2074A>G NP_015564.4:p.Arg692Gly
XR_938574.1:n.5217+9113T>C
NM_007325.5:c.2074A>G MANE Select NP_015564.5:p.Arg692Gly
NM_000828.5:c.2074A>G MANE Plus Clinical NP_000819.4:p.Arg692Gly