Canonical Allele Identifier: CA1083118490
Gene: GRIA1 HGNC NCBI

Linked Data

dbSNP Id: rs1753890133

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.153491271dup , CM000667.2:g.153491271dup GRCh38
NC_000005.9:g.152870831dup , CM000667.1:g.152870831dup GRCh37
NC_000005.8:g.152851024dup NCBI36
NG_047078.1:g.6576dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000340592.10:c.82+301dup ENSP00000339343.5:n.82+301dup
ENST00000520353.6:c.-126+301dup ENSP00000516539.1:n.-126+301dup
ENST00000706733.1:c.82+301dup ENSP00000516520.1:n.82+301dup
ENST00000706734.1:c.-38dup ENSP00000516521.1:n.-38dup
ENST00000706767.1:c.82+301dup ENSP00000516540.1:n.82+301dup
ENST00000285900.10:c.82+301dup MANE Select ENSP00000285900.4:n.82+301dup
ENST00000285900.9:c.82+301dup ENSP00000285900.4:n.82+301dup
ENST00000340592.9:c.82+301dup ENSP00000339343.5:n.82+301dup
ENST00000474198.1:n.327+301dup
ENST00000481559.6:n.223+1434dup
ENST00000517469.1:n.75dup
ENST00000518142.5:c.82+301dup ENSP00000427920.1:n.82+301dup
ENST00000518862.5:n.30+760dup
ENST00000520353.5:n.224+301dup
NM_000827.3:c.82+301dup NP_000818.2:n.82+301dup
NM_001114183.1:c.82+301dup NP_001107655.1:n.82+301dup
NM_001258019.1:c.82+301dup NP_001244948.1:n.82+301dup
NM_001258020.1:c.-261+301dup NP_001244949.1:n.-261+301dup
NR_047578.1:n.447+301dup
XM_011537635.1:c.22+1434dup XP_011535937.1:n.22+1434dup
XR_427776.2:n.352+301dup
NM_001364165.1:c.82+301dup NP_001351094.1:n.82+301dup
NM_001364166.1:c.-38dup NP_001351095.1:n.-38dup
NM_001364167.1:c.-187dup NP_001351096.1:n.-187dup
NR_157093.1:n.301+301dup
NM_000827.4:c.82+301dup MANE Select NP_000818.2:n.82+301dup
NM_001114183.2:c.82+301dup NP_001107655.1:n.82+301dup
NM_001258019.2:c.82+301dup NP_001244948.1:n.82+301dup
NM_001258020.2:c.-261+301dup NP_001244949.1:n.-261+301dup
NM_001364165.2:c.82+301dup NP_001351094.1:n.82+301dup
NM_001364166.2:c.-38dup NP_001351095.1:n.-38dup
NM_001364167.2:c.-187dup NP_001351096.1:n.-187dup
NR_047578.2:n.301+301dup
NR_157093.2:n.301+301dup