Canonical Allele Identifier: CA1592356837
Gene: GRIA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.153491364G= , CM000667.2:g.153491364G= GRCh38
NC_000005.9:g.152870924G= , CM000667.1:g.152870924G= GRCh37
NC_000005.8:g.152851117G= NCBI36
NG_047078.1:g.6669G=

Transcript Alleles

HGVS Amino-acid change
ENST00000340592.10:c.82+394G= ENSP00000339343.5:n.82+394G=
ENST00000520353.6:c.-126+394G= ENSP00000516539.1:n.-126+394G=
ENST00000706733.1:c.82+394G= ENSP00000516520.1:n.82+394G=
ENST00000706734.1:c.24+32G= ENSP00000516521.1:n.24+32G=
ENST00000706767.1:c.82+394G= ENSP00000516540.1:n.82+394G=
ENST00000285900.10:c.82+394G= MANE Select ENSP00000285900.4:n.82+394G=
ENST00000285900.9:c.82+394G= ENSP00000285900.4:n.82+394G=
ENST00000340592.9:c.82+394G= ENSP00000339343.5:n.82+394G=
ENST00000474198.1:n.327+394G=
ENST00000481559.6:n.223+1527G=
ENST00000517469.1:n.136+32G=
ENST00000518142.5:c.82+394G= ENSP00000427920.1:n.82+394G=
ENST00000518862.5:n.30+853G=
ENST00000520353.5:n.224+394G=
ENST00000521843.6:c.-126+32G= ENSP00000427864.2:n.-126+32G=
NM_000827.3:c.82+394G= NP_000818.2:n.82+394G=
NM_001114183.1:c.82+394G= NP_001107655.1:n.82+394G=
NM_001258019.1:c.82+394G= NP_001244948.1:n.82+394G=
NM_001258020.1:c.-261+394G= NP_001244949.1:n.-261+394G=
NM_001258023.1:c.-126+32G= NP_001244952.1:n.-126+32G=
NR_047578.1:n.447+394G=
XM_011537635.1:c.22+1527G= XP_011535937.1:n.22+1527G=
XR_427776.2:n.352+394G=
NM_001364165.1:c.82+394G= NP_001351094.1:n.82+394G=
NM_001364166.1:c.24+32G= NP_001351095.1:n.24+32G=
NM_001364167.1:c.-126+32G= NP_001351096.1:n.-126+32G=
NR_157093.1:n.301+394G=
NM_000827.4:c.82+394G= MANE Select NP_000818.2:n.82+394G=
NM_001114183.2:c.82+394G= NP_001107655.1:n.82+394G=
NM_001258019.2:c.82+394G= NP_001244948.1:n.82+394G=
NM_001258020.2:c.-261+394G= NP_001244949.1:n.-261+394G=
NM_001364165.2:c.82+394G= NP_001351094.1:n.82+394G=
NM_001364166.2:c.24+32G= NP_001351095.1:n.24+32G=
NM_001364167.2:c.-126+32G= NP_001351096.1:n.-126+32G=
NR_047578.2:n.301+394G=
NR_157093.2:n.301+394G=