Canonical Allele Identifier: CA2573055091

Gene: GRIA3

Linked Data

• ClinVar Variation Id: 1334442
• ClinVar RCV Id: RCV001814627
• dbSNP Id: rs2147401116

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123428101_123428103delinsTGT , CM000685.2:g.123428101_123428103delinsTGT	GRCh38
NC_000023.10:g.122561952_122561954delinsTGT , CM000685.1:g.122561952_122561954delinsTGT	GRCh37
NC_000023.9:g.122389633_122389635delinsTGT	NCBI36
NG_009377.2:g.248859_248861delinsTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.2038_2040delinsTGT MANE Select	ENSP00000478489.1:p.Gly680Cys
ENST00000622768.5:c.2038_2040delinsTGT MANE Plus Clinical	ENSP00000481554.1:p.Gly680Cys
ENST00000541091.5:c.2038_2040delinsTGT	ENSP00000446440.2:p.Gly680Cys
ENST00000620443.1:c.2038_2040delinsTGT	ENSP00000478489.1:p.Gly680Cys
ENST00000620581.4:c.2038_2040delinsTGT	ENSP00000481875.1:p.Gly680Cys
ENST00000622768.4:c.2038_2040delinsTGT	ENSP00000481554.1:p.Gly680Cys
NM_000828.4:c.2038_2040delinsTGT	NP_000819.3:p.Gly680Cys
NM_007325.4:c.2038_2040delinsTGT	NP_015564.4:p.Gly680Cys
XR_938574.1:n.5217+9147_5217+9149delinsACA
NM_007325.5:c.2038_2040delinsTGT MANE Select	NP_015564.5:p.Gly680Cys
NM_000828.5:c.2038_2040delinsTGT MANE Plus Clinical	NP_000819.4:p.Gly680Cys