Canonical Allele Identifier: CA12138728
Gene: GRIA1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2195450

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.153491449G>A , CM000667.2:g.153491449G>A GRCh38
NC_000005.9:g.152871009G>A , CM000667.1:g.152871009G>A GRCh37
NC_000005.8:g.152851202G>A NCBI36
NG_047078.1:g.6754G>A

Transcript Alleles

HGVS Amino-acid change
NM_000827.3:c.82+479G>A VV NP_000818.2:p.=
NM_001114183.1:c.82+479G>A VV NP_001107655.1:p.=
NM_001258019.1:c.82+479G>A VV NP_001244948.1:p.=
NM_001258020.1:c.-261+479G>A VV NP_001244949.1:p.=
NM_001258023.1:c.-126+117G>A VV NP_001244952.1:p.=
NR_047578.1:n.447+479G>A
XM_011537635.1:c.22+1612G>A XP_011535937.1:p.=
XR_427776.2:n.352+479G>A
NM_001364165.1:c.82+479G>A VV NP_001351094.1:p.=
NM_001364166.1:c.24+117G>A VV NP_001351095.1:p.=
NM_001364167.1:c.-126+117G>A VV NP_001351096.1:p.=
NR_157093.1:n.301+479G>A
NM_000827.4:c.82+479G>A VV MANE Preferred
ENST00000285900.9:c.82+479G>A ENSP00000285900.4:p.=
ENST00000340592.9:c.82+479G>A ENSP00000339343.5:p.=
ENST00000474198.1:n.327+479G>A
ENST00000481559.6:n.223+1612G>A
ENST00000517469.1:n.136+117G>A
ENST00000518142.5:c.82+479G>A ENSP00000427920.1:p.=
ENST00000518862.5:n.30+938G>A
ENST00000520353.5:n.224+479G>A
ENST00000521843.6:c.-126+117G>A ENSP00000427864.2:p.=