Canonical Allele Identifier: CA805861694

Gene: GRIA1

Linked Data

• dbSNP Id: rs1477174236
• gnomAD v3: 5-153491449-GAGA-G
• gnomAD v4: 5-153491449-GAGA-G
• MyVariant Identifiers: chr5:g.152871010_152871012del (hg19) ; chr5:g.153491450_153491452del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.153491455_153491457del , CM000667.2:g.153491455_153491457del	GRCh38
NC_000005.9:g.152871015_152871017del , CM000667.1:g.152871015_152871017del	GRCh37
NC_000005.8:g.152851208_152851210del	NCBI36
NG_047078.1:g.6760_6762del

Transcript Alleles

HGVS	Amino-acid change
ENST00000340592.10:c.82+485_82+487del	ENSP00000339343.5:n.82+485_82+487del
ENST00000520353.6:c.-126+485_-126+487del	ENSP00000516539.1:n.-126+485_-126+487del
ENST00000706733.1:c.82+485_82+487del	ENSP00000516520.1:n.82+485_82+487del
ENST00000706734.1:c.24+123_24+125del	ENSP00000516521.1:n.24+123_24+125del
ENST00000706767.1:c.82+485_82+487del	ENSP00000516540.1:n.82+485_82+487del
ENST00000285900.10:c.82+485_82+487del MANE Select	ENSP00000285900.4:n.82+485_82+487del
ENST00000285900.9:c.82+485_82+487del	ENSP00000285900.4:n.82+485_82+487del
ENST00000340592.9:c.82+485_82+487del	ENSP00000339343.5:n.82+485_82+487del
ENST00000474198.1:n.327+485_327+487del
ENST00000481559.6:n.223+1618_223+1620del
ENST00000517469.1:n.136+123_136+125del
ENST00000518142.5:c.82+485_82+487del	ENSP00000427920.1:n.82+485_82+487del
ENST00000518862.5:n.30+944_30+946del
ENST00000520353.5:n.224+485_224+487del
ENST00000521843.6:c.-126+123_-126+125del	ENSP00000427864.2:n.-126+123_-126+125del
NM_000827.3:c.82+485_82+487del	NP_000818.2:n.82+485_82+487del
NM_001114183.1:c.82+485_82+487del	NP_001107655.1:n.82+485_82+487del
NM_001258019.1:c.82+485_82+487del	NP_001244948.1:n.82+485_82+487del
NM_001258020.1:c.-261+485_-261+487del	NP_001244949.1:n.-261+485_-261+487del
NM_001258023.1:c.-126+123_-126+125del	NP_001244952.1:n.-126+123_-126+125del
NR_047578.1:n.447+485_447+487del
XM_011537635.1:c.22+1618_22+1620del	XP_011535937.1:n.22+1618_22+1620del
XR_427776.2:n.352+485_352+487del
NM_001364165.1:c.82+485_82+487del	NP_001351094.1:n.82+485_82+487del
NM_001364166.1:c.24+123_24+125del	NP_001351095.1:n.24+123_24+125del
NM_001364167.1:c.-126+123_-126+125del	NP_001351096.1:n.-126+123_-126+125del
NR_157093.1:n.301+485_301+487del
NM_000827.4:c.82+485_82+487del MANE Select	NP_000818.2:n.82+485_82+487del
NM_001114183.2:c.82+485_82+487del	NP_001107655.1:n.82+485_82+487del
NM_001258019.2:c.82+485_82+487del	NP_001244948.1:n.82+485_82+487del
NM_001258020.2:c.-261+485_-261+487del	NP_001244949.1:n.-261+485_-261+487del
NM_001364165.2:c.82+485_82+487del	NP_001351094.1:n.82+485_82+487del
NM_001364166.2:c.24+123_24+125del	NP_001351095.1:n.24+123_24+125del
NM_001364167.2:c.-126+123_-126+125del	NP_001351096.1:n.-126+123_-126+125del
NR_047578.2:n.301+485_301+487del
NR_157093.2:n.301+485_301+487del