Canonical Allele Identifier: CA2694611829

Gene: GRIA3

Linked Data

• gnomAD v4: X-123427799-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123427799G>C , CM000685.2:g.123427799G>C	GRCh38
NC_000023.10:g.122561650G>C , CM000685.1:g.122561650G>C	GRCh37
NC_000023.9:g.122389331G>C	NCBI36
NG_009377.2:g.248557G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.1878-142G>C MANE Select	ENSP00000478489.1:n.1878-142G>C
ENST00000622768.5:c.1878-142G>C MANE Plus Clinical	ENSP00000481554.1:n.1878-142G>C
ENST00000541091.5:c.1878-142G>C	ENSP00000446440.2:n.1878-142G>C
ENST00000620443.1:c.1878-142G>C	ENSP00000478489.1:n.1878-142G>C
ENST00000620581.4:c.1878-142G>C	ENSP00000481875.1:n.1878-142G>C
ENST00000622768.4:c.1878-142G>C	ENSP00000481554.1:n.1878-142G>C
NM_000828.4:c.1878-142G>C	NP_000819.3:n.1878-142G>C
NM_007325.4:c.1878-142G>C	NP_015564.4:n.1878-142G>C
XR_938574.1:n.5217+9451C>G
NM_007325.5:c.1878-142G>C MANE Select	NP_015564.5:n.1878-142G>C
NM_000828.5:c.1878-142G>C MANE Plus Clinical	NP_000819.4:n.1878-142G>C