Canonical Allele Identifier: CA414259567

Gene: GRIA3

Linked Data

• MyVariant Identifiers: chrX:g.122561809T>G (hg19) ; chrX:g.123427958T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123427958T>G , CM000685.2:g.123427958T>G	GRCh38
NC_000023.10:g.122561809T>G , CM000685.1:g.122561809T>G	GRCh37
NC_000023.9:g.122389490T>G	NCBI36
NG_009377.2:g.248716T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.1895T>G MANE Select	ENSP00000478489.1:p.Ile632Ser
ENST00000622768.5:c.1895T>G MANE Plus Clinical	ENSP00000481554.1:p.Ile632Ser
ENST00000541091.5:c.1895T>G	ENSP00000446440.2:p.Ile632Ser
ENST00000620443.1:c.1895T>G	ENSP00000478489.1:p.Ile632Ser
ENST00000620581.4:c.1895T>G	ENSP00000481875.1:p.Ile632Ser
ENST00000622768.4:c.1895T>G	ENSP00000481554.1:p.Ile632Ser
NM_000828.4:c.1895T>G	NP_000819.3:p.Ile632Ser
NM_007325.4:c.1895T>G	NP_015564.4:p.Ile632Ser
XR_938574.1:n.5217+9292A>C
NM_007325.5:c.1895T>G MANE Select	NP_015564.5:p.Ile632Ser
NM_000828.5:c.1895T>G MANE Plus Clinical	NP_000819.4:p.Ile632Ser