Canonical Allele Identifier: CA2739273742

Gene: GRIA3

Linked Data

• ClinVar Variation Id: 2867290
• ClinVar RCV Id: RCV003700650

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123428151_123428152delinsAA , CM000685.2:g.123428151_123428152delinsAA	GRCh38
NC_000023.10:g.122562002_122562003delinsAA , CM000685.1:g.122562002_122562003delinsAA	GRCh37
NC_000023.9:g.122389683_122389684delinsAA	NCBI36
NG_009377.2:g.248909_248910delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.2076+12_2076+13delinsAA MANE Select	ENSP00000478489.1:n.2076+12_2076+13delinsAA
ENST00000622768.5:c.2076+12_2076+13delinsAA MANE Plus Clinical	ENSP00000481554.1:n.2076+12_2076+13delinsAA
ENST00000541091.5:c.2076+12_2076+13delinsAA	ENSP00000446440.2:n.2076+12_2076+13delinsAA
ENST00000620443.1:c.2076+12_2076+13delinsAA	ENSP00000478489.1:n.2076+12_2076+13delinsAA
ENST00000620581.4:c.2076+12_2076+13delinsAA	ENSP00000481875.1:n.2076+12_2076+13delinsAA
ENST00000622768.4:c.2076+12_2076+13delinsAA	ENSP00000481554.1:n.2076+12_2076+13delinsAA
NM_000828.4:c.2076+12_2076+13delinsAA	NP_000819.3:n.2076+12_2076+13delinsAA
NM_007325.4:c.2076+12_2076+13delinsAA	NP_015564.4:n.2076+12_2076+13delinsAA
XR_938574.1:n.5217+9098_5217+9099delinsTT
NM_007325.5:c.2076+12_2076+13delinsAA MANE Select	NP_015564.5:n.2076+12_2076+13delinsAA
NM_000828.5:c.2076+12_2076+13delinsAA MANE Plus Clinical	NP_000819.4:n.2076+12_2076+13delinsAA