Canonical Allele Identifier: CA2676119339
Gene: GRIA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.153491235C>G , CM000667.2:g.153491235C>G GRCh38
NC_000005.9:g.152870795C>G , CM000667.1:g.152870795C>G GRCh37
NC_000005.8:g.152850988C>G NCBI36
NG_047078.1:g.6540C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000340592.10:c.82+265C>G ENSP00000339343.5:n.82+265C>G
ENST00000520353.6:c.-126+265C>G ENSP00000516539.1:n.-126+265C>G
ENST00000706733.1:c.82+265C>G ENSP00000516520.1:n.82+265C>G
ENST00000706734.1:c.-74C>G ENSP00000516521.1:n.-74C>G
ENST00000706767.1:c.82+265C>G ENSP00000516540.1:n.82+265C>G
ENST00000285900.10:c.82+265C>G MANE Select ENSP00000285900.4:n.82+265C>G
ENST00000285900.9:c.82+265C>G ENSP00000285900.4:n.82+265C>G
ENST00000340592.9:c.82+265C>G ENSP00000339343.5:n.82+265C>G
ENST00000474198.1:n.327+265C>G
ENST00000481559.6:n.223+1398C>G
ENST00000517469.1:n.39C>G
ENST00000518142.5:c.82+265C>G ENSP00000427920.1:n.82+265C>G
ENST00000518862.5:n.30+724C>G
ENST00000520353.5:n.224+265C>G
NM_000827.3:c.82+265C>G NP_000818.2:n.82+265C>G
NM_001114183.1:c.82+265C>G NP_001107655.1:n.82+265C>G
NM_001258019.1:c.82+265C>G NP_001244948.1:n.82+265C>G
NM_001258020.1:c.-261+265C>G NP_001244949.1:n.-261+265C>G
NR_047578.1:n.447+265C>G
XM_011537635.1:c.22+1398C>G XP_011535937.1:n.22+1398C>G
XR_427776.2:n.352+265C>G
NM_001364165.1:c.82+265C>G NP_001351094.1:n.82+265C>G
NM_001364166.1:c.-74C>G NP_001351095.1:n.-74C>G
NM_001364167.1:c.-223C>G NP_001351096.1:n.-223C>G
NR_157093.1:n.301+265C>G
NM_000827.4:c.82+265C>G MANE Select NP_000818.2:n.82+265C>G
NM_001114183.2:c.82+265C>G NP_001107655.1:n.82+265C>G
NM_001258019.2:c.82+265C>G NP_001244948.1:n.82+265C>G
NM_001258020.2:c.-261+265C>G NP_001244949.1:n.-261+265C>G
NM_001364165.2:c.82+265C>G NP_001351094.1:n.82+265C>G
NM_001364166.2:c.-74C>G NP_001351095.1:n.-74C>G
NM_001364167.2:c.-223C>G NP_001351096.1:n.-223C>G
NR_047578.2:n.301+265C>G
NR_157093.2:n.301+265C>G