Canonical Allele Identifier: CA2455873784

Gene: GRIA3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123361111C= , CM000685.2:g.123361111C=	GRCh38
NC_000023.10:g.122494962C= , CM000685.1:g.122494962C=	GRCh37
NC_000023.9:g.122322643C=	NCBI36
NG_009377.2:g.181869C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.750+6148C= MANE Select	ENSP00000478489.1:n.750+6148C=
ENST00000622768.5:c.750+6148C= MANE Plus Clinical	ENSP00000481554.1:n.750+6148C=
ENST00000477389.1:n.426-132C=
ENST00000541091.5:c.750+6148C=	ENSP00000446440.2:n.750+6148C=
ENST00000620443.1:c.750+6148C=	ENSP00000478489.1:n.750+6148C=
ENST00000620581.4:c.750+6148C=	ENSP00000481875.1:n.750+6148C=
ENST00000622768.4:c.750+6148C=	ENSP00000481554.1:n.750+6148C=
NM_000828.4:c.750+6148C=	NP_000819.3:n.750+6148C=
NM_007325.4:c.750+6148C=	NP_015564.4:n.750+6148C=
NM_007325.5:c.750+6148C= MANE Select	NP_015564.5:n.750+6148C=
NM_000828.5:c.750+6148C= MANE Plus Clinical	NP_000819.4:n.750+6148C=