Canonical Allele Identifier: CA1592356775

Gene: GRIA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.153491259G= , CM000667.2:g.153491259G=	GRCh38
NC_000005.9:g.152870819G= , CM000667.1:g.152870819G=	GRCh37
NC_000005.8:g.152851012G=	NCBI36
NG_047078.1:g.6564G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340592.10:c.82+289G=	ENSP00000339343.5:n.82+289G=
ENST00000520353.6:c.-126+289G=	ENSP00000516539.1:n.-126+289G=
ENST00000706733.1:c.82+289G=	ENSP00000516520.1:n.82+289G=
ENST00000706734.1:c.-50G=	ENSP00000516521.1:n.-50G=
ENST00000706767.1:c.82+289G=	ENSP00000516540.1:n.82+289G=
ENST00000285900.10:c.82+289G= MANE Select	ENSP00000285900.4:n.82+289G=
ENST00000285900.9:c.82+289G=	ENSP00000285900.4:n.82+289G=
ENST00000340592.9:c.82+289G=	ENSP00000339343.5:n.82+289G=
ENST00000474198.1:n.327+289G=
ENST00000481559.6:n.223+1422G=
ENST00000517469.1:n.63G=
ENST00000518142.5:c.82+289G=	ENSP00000427920.1:n.82+289G=
ENST00000518862.5:n.30+748G=
ENST00000520353.5:n.224+289G=
NM_000827.3:c.82+289G=	NP_000818.2:n.82+289G=
NM_001114183.1:c.82+289G=	NP_001107655.1:n.82+289G=
NM_001258019.1:c.82+289G=	NP_001244948.1:n.82+289G=
NM_001258020.1:c.-261+289G=	NP_001244949.1:n.-261+289G=
NR_047578.1:n.447+289G=
XM_011537635.1:c.22+1422G=	XP_011535937.1:n.22+1422G=
XR_427776.2:n.352+289G=
NM_001364165.1:c.82+289G=	NP_001351094.1:n.82+289G=
NM_001364166.1:c.-50G=	NP_001351095.1:n.-50G=
NM_001364167.1:c.-199G=	NP_001351096.1:n.-199G=
NR_157093.1:n.301+289G=
NM_000827.4:c.82+289G= MANE Select	NP_000818.2:n.82+289G=
NM_001114183.2:c.82+289G=	NP_001107655.1:n.82+289G=
NM_001258019.2:c.82+289G=	NP_001244948.1:n.82+289G=
NM_001258020.2:c.-261+289G=	NP_001244949.1:n.-261+289G=
NM_001364165.2:c.82+289G=	NP_001351094.1:n.82+289G=
NM_001364166.2:c.-50G=	NP_001351095.1:n.-50G=
NM_001364167.2:c.-199G=	NP_001351096.1:n.-199G=
NR_047578.2:n.301+289G=
NR_157093.2:n.301+289G=