Canonical Allele Identifier: CA335232842
Gene: GRIA3 HGNC NCBI

Linked Data

dbSNP Id: rs986132536
gnomAD v2: X-122441516-C-A
gnomAD v3: X-123307665-C-A
gnomAD v4: X-123307665-C-A
MyVariant Identifiers: chrX:g.122441516C>A (hg19) chrX:g.123307665C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.123307665C>A , CM000685.2:g.123307665C>A GRCh38
NC_000023.10:g.122441516C>A , CM000685.1:g.122441516C>A GRCh37
NC_000023.9:g.122269197C>A NCBI36
NG_009377.2:g.128423C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000620443.2:c.509-18361C>A MANE Select ENSP00000478489.1:n.509-18361C>A
ENST00000622768.5:c.509-18361C>A MANE Plus Clinical ENSP00000481554.1:n.509-18361C>A
ENST00000541091.5:c.509-18361C>A ENSP00000446440.2:n.509-18361C>A
ENST00000620443.1:c.509-18361C>A ENSP00000478489.1:n.509-18361C>A
ENST00000620581.4:c.509-18361C>A ENSP00000481875.1:n.509-18361C>A
ENST00000622768.4:c.509-18361C>A ENSP00000481554.1:n.509-18361C>A
NM_000828.4:c.509-18361C>A NP_000819.3:n.509-18361C>A
NM_007325.4:c.509-18361C>A NP_015564.4:n.509-18361C>A
NM_007325.5:c.509-18361C>A MANE Select NP_015564.5:n.509-18361C>A
NM_000828.5:c.509-18361C>A MANE Plus Clinical NP_000819.4:n.509-18361C>A
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