Canonical Allele Identifier: CA1592442984

Gene: GRIA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.153677988C= , CM000667.2:g.153677988C=	GRCh38
NC_000005.9:g.153057548C= , CM000667.1:g.153057548C=	GRCh37
NC_000005.8:g.153037741C=	NCBI36
NG_047078.1:g.193293C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000827.4:c.1029+827C= MANE Select	NP_000818.2:n.1029+827C=
ENST00000285900.10:c.1029+827C= MANE Select	ENSP00000285900.4:n.1029+827C=
NM_000827.3:c.1029+827C=	NP_000818.2:n.1029+827C=
NM_001114183.1:c.1029+827C=	NP_001107655.1:n.1029+827C=
NM_001114183.2:c.1029+827C=	NP_001107655.1:n.1029+827C=
NM_001258019.1:c.789+827C=	NP_001244948.1:n.789+827C=
NM_001258019.2:c.789+827C=	NP_001244948.1:n.789+827C=
NM_001258020.1:c.744+827C=	NP_001244949.1:n.744+827C=
NM_001258020.2:c.744+827C=	NP_001244949.1:n.744+827C=
NM_001258021.1:c.1059+827C=	NP_001244950.1:n.1059+827C=
NM_001258021.2:c.1059+827C=	NP_001244950.1:n.1059+827C=
NM_001258022.1:c.1059+827C=	NP_001244951.1:n.1059+827C=
NM_001258022.2:c.1059+827C=	NP_001244951.1:n.1059+827C=
NM_001258023.1:c.822+827C=	NP_001244952.1:n.822+827C=
NM_001364165.1:c.861+3327C=	NP_001351094.1:n.861+3327C=
NM_001364165.2:c.861+3327C=	NP_001351094.1:n.861+3327C=
NM_001364166.1:c.1056+827C=	NP_001351095.1:n.1056+827C=
NM_001364166.2:c.1056+827C=	NP_001351095.1:n.1056+827C=
NM_001364167.1:c.822+827C=	NP_001351096.1:n.822+827C=
NM_001364167.2:c.822+827C=	NP_001351096.1:n.822+827C=
NR_047578.1:n.1256+827C=
NR_047578.2:n.1110+827C=
NR_157093.1:n.1248+827C=
NR_157093.2:n.1248+827C=
ENST00000285900.9:c.1029+827C=	ENSP00000285900.4:n.1029+827C=
ENST00000340592.10:c.1029+827C=	ENSP00000339343.5:n.1029+827C=
ENST00000340592.9:c.1029+827C=	ENSP00000339343.5:n.1029+827C=
ENST00000448073.8:c.1059+827C=	ENSP00000415569.2:n.1059+827C=
ENST00000481559.6:n.1170+827C=
ENST00000518142.5:c.789+827C=	ENSP00000427920.1:n.789+827C=
ENST00000518783.1:c.1059+827C=	ENSP00000428994.1:n.1059+827C=
ENST00000521843.6:c.822+827C=	ENSP00000427864.2:n.822+827C=
ENST00000706733.1:c.1029+827C=	ENSP00000516520.1:n.1029+827C=
ENST00000706734.1:c.1056+827C=	ENSP00000516521.1:n.1056+827C=
XM_011537635.1:c.969+827C=	XP_011535937.1:n.969+827C=
XM_017009392.1:c.1059+827C=	XP_016864881.1:n.1059+827C=
XR_427776.2:n.1299+827C=