Canonical Allele Identifier: CA2694612040

Gene: GRIA3

Linked Data

• gnomAD v4: X-123428140-G-GCACT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123428140_123428141insCACT , CM000685.2:g.123428140_123428141insCACT	GRCh38
NC_000023.10:g.122561991_122561992insCACT , CM000685.1:g.122561991_122561992insCACT	GRCh37
NC_000023.9:g.122389672_122389673insCACT	NCBI36
NG_009377.2:g.248898_248899insCACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.2076+1_2076+2insCACT MANE Select	ENSP00000478489.1:n.2076+1_2076+2insCACT
ENST00000622768.5:c.2076+1_2076+2insCACT MANE Plus Clinical	ENSP00000481554.1:n.2076+1_2076+2insCACT
ENST00000541091.5:c.2076+1_2076+2insCACT	ENSP00000446440.2:n.2076+1_2076+2insCACT
ENST00000620443.1:c.2076+1_2076+2insCACT	ENSP00000478489.1:n.2076+1_2076+2insCACT
ENST00000620581.4:c.2076+1_2076+2insCACT	ENSP00000481875.1:n.2076+1_2076+2insCACT
ENST00000622768.4:c.2076+1_2076+2insCACT	ENSP00000481554.1:n.2076+1_2076+2insCACT
NM_000828.4:c.2076+1_2076+2insCACT	NP_000819.3:n.2076+1_2076+2insCACT
NM_007325.4:c.2076+1_2076+2insCACT	NP_015564.4:n.2076+1_2076+2insCACT
XR_938574.1:n.5217+9109_5217+9110insAGTG
NM_007325.5:c.2076+1_2076+2insCACT MANE Select	NP_015564.5:n.2076+1_2076+2insCACT
NM_000828.5:c.2076+1_2076+2insCACT MANE Plus Clinical	NP_000819.4:n.2076+1_2076+2insCACT