Canonical Allele Identifier: CA2455857808

Gene: GRIA3

Linked Data

• dbSNP Id: rs2044763364

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123307648G>A , CM000685.2:g.123307648G>A	GRCh38
NC_000023.10:g.122441499G>A , CM000685.1:g.122441499G>A	GRCh37
NC_000023.9:g.122269180G>A	NCBI36
NG_009377.2:g.128406G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000620443.2:c.509-18378G>A MANE Select	ENSP00000478489.1:n.509-18378G>A
ENST00000622768.5:c.509-18378G>A MANE Plus Clinical	ENSP00000481554.1:n.509-18378G>A
ENST00000541091.5:c.509-18378G>A	ENSP00000446440.2:n.509-18378G>A
ENST00000620443.1:c.509-18378G>A	ENSP00000478489.1:n.509-18378G>A
ENST00000620581.4:c.509-18378G>A	ENSP00000481875.1:n.509-18378G>A
ENST00000622768.4:c.509-18378G>A	ENSP00000481554.1:n.509-18378G>A
NM_000828.4:c.509-18378G>A	NP_000819.3:n.509-18378G>A
NM_007325.4:c.509-18378G>A	NP_015564.4:n.509-18378G>A
NM_007325.5:c.509-18378G>A MANE Select	NP_015564.5:n.509-18378G>A
NM_000828.5:c.509-18378G>A MANE Plus Clinical	NP_000819.4:n.509-18378G>A