Canonical Allele Identifier: CA2676119611

Gene: GRIA1

Linked Data

• gnomAD v4: 5-153491469-G-GCAATATACCCAGCACCCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.153491470_153491471insAATATACCCAGCACCCCTC , CM000667.2:g.153491470_153491471insAATATACCCAGCACCCCTC	GRCh38
NC_000005.9:g.152871030_152871031insAATATACCCAGCACCCCTC , CM000667.1:g.152871030_152871031insAATATACCCAGCACCCCTC	GRCh37
NC_000005.8:g.152851223_152851224insAATATACCCAGCACCCCTC	NCBI36
NG_047078.1:g.6775_6776insAATATACCCAGCACCCCTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000340592.10:c.82+500_82+501insAATATACCCAGCACCCCTC	ENSP00000339343.5:n.82+500_82+501insAATATACCCAGCACCCCTC
ENST00000520353.6:c.-126+500_-126+501insAATATACCCAGCACCCCTC	ENSP00000516539.1:n.-126+500_-126+501insAATATACCCAGCACCCCTC
ENST00000706733.1:c.82+500_82+501insAATATACCCAGCACCCCTC	ENSP00000516520.1:n.82+500_82+501insAATATACCCAGCACCCCTC
ENST00000706734.1:c.24+138_24+139insAATATACCCAGCACCCCTC	ENSP00000516521.1:n.24+138_24+139insAATATACCCAGCACCCCTC
ENST00000706767.1:c.82+500_82+501insAATATACCCAGCACCCCTC	ENSP00000516540.1:n.82+500_82+501insAATATACCCAGCACCCCTC
ENST00000285900.10:c.82+500_82+501insAATATACCCAGCACCCCTC MANE Select	ENSP00000285900.4:n.82+500_82+501insAATATACCCAGCACCCCTC
ENST00000285900.9:c.82+500_82+501insAATATACCCAGCACCCCTC	ENSP00000285900.4:n.82+500_82+501insAATATACCCAGCACCCCTC
ENST00000340592.9:c.82+500_82+501insAATATACCCAGCACCCCTC	ENSP00000339343.5:n.82+500_82+501insAATATACCCAGCACCCCTC
ENST00000474198.1:n.327+500_327+501insAATATACCCAGCACCCCTC
ENST00000481559.6:n.223+1633_223+1634insAATATACCCAGCACCCCTC
ENST00000517469.1:n.136+138_136+139insAATATACCCAGCACCCCTC
ENST00000518142.5:c.82+500_82+501insAATATACCCAGCACCCCTC	ENSP00000427920.1:n.82+500_82+501insAATATACCCAGCACCCCTC
ENST00000518862.5:n.30+959_30+960insAATATACCCAGCACCCCTC
ENST00000520353.5:n.224+500_224+501insAATATACCCAGCACCCCTC
ENST00000521843.6:c.-126+138_-126+139insAATATACCCAGCACCCCTC	ENSP00000427864.2:n.-126+138_-126+139insAATATACCCAGCACCCCTC
NM_000827.3:c.82+500_82+501insAATATACCCAGCACCCCTC	NP_000818.2:n.82+500_82+501insAATATACCCAGCACCCCTC
NM_001114183.1:c.82+500_82+501insAATATACCCAGCACCCCTC	NP_001107655.1:n.82+500_82+501insAATATACCCAGCACCCCTC
NM_001258019.1:c.82+500_82+501insAATATACCCAGCACCCCTC	NP_001244948.1:n.82+500_82+501insAATATACCCAGCACCCCTC
NM_001258020.1:c.-261+500_-261+501insAATATACCCAGCACCCCTC	NP_001244949.1:n.-261+500_-261+501insAATATACCCAGCACCCCTC
NM_001258023.1:c.-126+138_-126+139insAATATACCCAGCACCCCTC	NP_001244952.1:n.-126+138_-126+139insAATATACCCAGCACCCCTC
NR_047578.1:n.447+500_447+501insAATATACCCAGCACCCCTC
XM_011537635.1:c.22+1633_22+1634insAATATACCCAGCACCCCTC	XP_011535937.1:n.22+1633_22+1634insAATATACCCAGCACCCCTC
XR_427776.2:n.352+500_352+501insAATATACCCAGCACCCCTC
NM_001364165.1:c.82+500_82+501insAATATACCCAGCACCCCTC	NP_001351094.1:n.82+500_82+501insAATATACCCAGCACCCCTC
NM_001364166.1:c.24+138_24+139insAATATACCCAGCACCCCTC	NP_001351095.1:n.24+138_24+139insAATATACCCAGCACCCCTC
NM_001364167.1:c.-126+138_-126+139insAATATACCCAGCACCCCTC	NP_001351096.1:n.-126+138_-126+139insAATATACCCAGCACCCCTC
NR_157093.1:n.301+500_301+501insAATATACCCAGCACCCCTC
NM_000827.4:c.82+500_82+501insAATATACCCAGCACCCCTC MANE Select	NP_000818.2:n.82+500_82+501insAATATACCCAGCACCCCTC
NM_001114183.2:c.82+500_82+501insAATATACCCAGCACCCCTC	NP_001107655.1:n.82+500_82+501insAATATACCCAGCACCCCTC
NM_001258019.2:c.82+500_82+501insAATATACCCAGCACCCCTC	NP_001244948.1:n.82+500_82+501insAATATACCCAGCACCCCTC
NM_001258020.2:c.-261+500_-261+501insAATATACCCAGCACCCCTC	NP_001244949.1:n.-261+500_-261+501insAATATACCCAGCACCCCTC
NM_001364165.2:c.82+500_82+501insAATATACCCAGCACCCCTC	NP_001351094.1:n.82+500_82+501insAATATACCCAGCACCCCTC
NM_001364166.2:c.24+138_24+139insAATATACCCAGCACCCCTC	NP_001351095.1:n.24+138_24+139insAATATACCCAGCACCCCTC
NM_001364167.2:c.-126+138_-126+139insAATATACCCAGCACCCCTC	NP_001351096.1:n.-126+138_-126+139insAATATACCCAGCACCCCTC
NR_047578.2:n.301+500_301+501insAATATACCCAGCACCCCTC
NR_157093.2:n.301+500_301+501insAATATACCCAGCACCCCTC