Canonical Allele Identifier: CA2526411918
Gene: GRIA3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.123307499C>A , CM000685.2:g.123307499C>A GRCh38
NC_000023.10:g.122441350C>A , CM000685.1:g.122441350C>A GRCh37
NC_000023.9:g.122269031C>A NCBI36
NG_009377.2:g.128257C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000620443.2:c.509-18527C>A MANE Select ENSP00000478489.1:n.509-18527C>A
ENST00000622768.5:c.509-18527C>A MANE Plus Clinical ENSP00000481554.1:n.509-18527C>A
ENST00000541091.5:c.509-18527C>A ENSP00000446440.2:n.509-18527C>A
ENST00000620443.1:c.509-18527C>A ENSP00000478489.1:n.509-18527C>A
ENST00000620581.4:c.509-18527C>A ENSP00000481875.1:n.509-18527C>A
ENST00000622768.4:c.509-18527C>A ENSP00000481554.1:n.509-18527C>A
NM_000828.4:c.509-18527C>A NP_000819.3:n.509-18527C>A
NM_007325.4:c.509-18527C>A NP_015564.4:n.509-18527C>A
NM_007325.5:c.509-18527C>A MANE Select NP_015564.5:n.509-18527C>A
NM_000828.5:c.509-18527C>A MANE Plus Clinical NP_000819.4:n.509-18527C>A
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