Canonical Allele Identifier: CA414260203

Gene: GRIA3

Linked Data

• MyVariant Identifiers: chrX:g.122561956C>G (hg19) ; chrX:g.123428105C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123428105C>G , CM000685.2:g.123428105C>G	GRCh38
NC_000023.10:g.122561956C>G , CM000685.1:g.122561956C>G	GRCh37
NC_000023.9:g.122389637C>G	NCBI36
NG_009377.2:g.248863C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.2042C>G MANE Select	ENSP00000478489.1:p.Thr681Ser
ENST00000622768.5:c.2042C>G MANE Plus Clinical	ENSP00000481554.1:p.Thr681Ser
ENST00000541091.5:c.2042C>G	ENSP00000446440.2:p.Thr681Ser
ENST00000620443.1:c.2042C>G	ENSP00000478489.1:p.Thr681Ser
ENST00000620581.4:c.2042C>G	ENSP00000481875.1:p.Thr681Ser
ENST00000622768.4:c.2042C>G	ENSP00000481554.1:p.Thr681Ser
NM_000828.4:c.2042C>G	NP_000819.3:p.Thr681Ser
NM_007325.4:c.2042C>G	NP_015564.4:p.Thr681Ser
XR_938574.1:n.5217+9145G>C
NM_007325.5:c.2042C>G MANE Select	NP_015564.5:p.Thr681Ser
NM_000828.5:c.2042C>G MANE Plus Clinical	NP_000819.4:p.Thr681Ser