Canonical Allele Identifier: CA1592356832

Gene: GRIA1

Linked Data

• dbSNP Id: rs1753899826

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.153491352_153491355del , CM000667.2:g.153491352_153491355del	GRCh38
NC_000005.9:g.152870912_152870915del , CM000667.1:g.152870912_152870915del	GRCh37
NC_000005.8:g.152851105_152851108del	NCBI36
NG_047078.1:g.6657_6660del

Transcript Alleles

HGVS	Amino-acid change
ENST00000340592.10:c.82+382_82+385del	ENSP00000339343.5:n.82+382_82+385del
ENST00000520353.6:c.-126+382_-126+385del	ENSP00000516539.1:n.-126+382_-126+385del
ENST00000706733.1:c.82+382_82+385del	ENSP00000516520.1:n.82+382_82+385del
ENST00000706734.1:c.24+20_24+23del	ENSP00000516521.1:n.24+20_24+23del
ENST00000706767.1:c.82+382_82+385del	ENSP00000516540.1:n.82+382_82+385del
ENST00000285900.10:c.82+382_82+385del MANE Select	ENSP00000285900.4:n.82+382_82+385del
ENST00000285900.9:c.82+382_82+385del	ENSP00000285900.4:n.82+382_82+385del
ENST00000340592.9:c.82+382_82+385del	ENSP00000339343.5:n.82+382_82+385del
ENST00000474198.1:n.327+382_327+385del
ENST00000481559.6:n.223+1515_223+1518del
ENST00000517469.1:n.136+20_136+23del
ENST00000518142.5:c.82+382_82+385del	ENSP00000427920.1:n.82+382_82+385del
ENST00000518862.5:n.30+841_30+844del
ENST00000520353.5:n.224+382_224+385del
ENST00000521843.6:c.-126+20_-126+23del	ENSP00000427864.2:n.-126+20_-126+23del
NM_000827.3:c.82+382_82+385del	NP_000818.2:n.82+382_82+385del
NM_001114183.1:c.82+382_82+385del	NP_001107655.1:n.82+382_82+385del
NM_001258019.1:c.82+382_82+385del	NP_001244948.1:n.82+382_82+385del
NM_001258020.1:c.-261+382_-261+385del	NP_001244949.1:n.-261+382_-261+385del
NM_001258023.1:c.-126+20_-126+23del	NP_001244952.1:n.-126+20_-126+23del
NR_047578.1:n.447+382_447+385del
XM_011537635.1:c.22+1515_22+1518del	XP_011535937.1:n.22+1515_22+1518del
XR_427776.2:n.352+382_352+385del
NM_001364165.1:c.82+382_82+385del	NP_001351094.1:n.82+382_82+385del
NM_001364166.1:c.24+20_24+23del	NP_001351095.1:n.24+20_24+23del
NM_001364167.1:c.-126+20_-126+23del	NP_001351096.1:n.-126+20_-126+23del
NR_157093.1:n.301+382_301+385del
NM_000827.4:c.82+382_82+385del MANE Select	NP_000818.2:n.82+382_82+385del
NM_001114183.2:c.82+382_82+385del	NP_001107655.1:n.82+382_82+385del
NM_001258019.2:c.82+382_82+385del	NP_001244948.1:n.82+382_82+385del
NM_001258020.2:c.-261+382_-261+385del	NP_001244949.1:n.-261+382_-261+385del
NM_001364165.2:c.82+382_82+385del	NP_001351094.1:n.82+382_82+385del
NM_001364166.2:c.24+20_24+23del	NP_001351095.1:n.24+20_24+23del
NM_001364167.2:c.-126+20_-126+23del	NP_001351096.1:n.-126+20_-126+23del
NR_047578.2:n.301+382_301+385del
NR_157093.2:n.301+382_301+385del