Canonical Allele Identifier: CA2676119459

Gene: GRIA1

Linked Data

• gnomAD v4: 5-153491382-TATGCAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.153491385_153491390del , CM000667.2:g.153491385_153491390del	GRCh38
NC_000005.9:g.152870945_152870950del , CM000667.1:g.152870945_152870950del	GRCh37
NC_000005.8:g.152851138_152851143del	NCBI36
NG_047078.1:g.6690_6695del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340592.10:c.82+415_82+420del	ENSP00000339343.5:n.82+415_82+420del
ENST00000520353.6:c.-126+415_-126+420del	ENSP00000516539.1:n.-126+415_-126+420del
ENST00000706733.1:c.82+415_82+420del	ENSP00000516520.1:n.82+415_82+420del
ENST00000706734.1:c.24+53_24+58del	ENSP00000516521.1:n.24+53_24+58del
ENST00000706767.1:c.82+415_82+420del	ENSP00000516540.1:n.82+415_82+420del
ENST00000285900.10:c.82+415_82+420del MANE Select	ENSP00000285900.4:n.82+415_82+420del
ENST00000285900.9:c.82+415_82+420del	ENSP00000285900.4:n.82+415_82+420del
ENST00000340592.9:c.82+415_82+420del	ENSP00000339343.5:n.82+415_82+420del
ENST00000474198.1:n.327+415_327+420del
ENST00000481559.6:n.223+1548_223+1553del
ENST00000517469.1:n.136+53_136+58del
ENST00000518142.5:c.82+415_82+420del	ENSP00000427920.1:n.82+415_82+420del
ENST00000518862.5:n.30+874_30+879del
ENST00000520353.5:n.224+415_224+420del
ENST00000521843.6:c.-126+53_-126+58del	ENSP00000427864.2:n.-126+53_-126+58del
NM_000827.3:c.82+415_82+420del	NP_000818.2:n.82+415_82+420del
NM_001114183.1:c.82+415_82+420del	NP_001107655.1:n.82+415_82+420del
NM_001258019.1:c.82+415_82+420del	NP_001244948.1:n.82+415_82+420del
NM_001258020.1:c.-261+415_-261+420del	NP_001244949.1:n.-261+415_-261+420del
NM_001258023.1:c.-126+53_-126+58del	NP_001244952.1:n.-126+53_-126+58del
NR_047578.1:n.447+415_447+420del
XM_011537635.1:c.22+1548_22+1553del	XP_011535937.1:n.22+1548_22+1553del
XR_427776.2:n.352+415_352+420del
NM_001364165.1:c.82+415_82+420del	NP_001351094.1:n.82+415_82+420del
NM_001364166.1:c.24+53_24+58del	NP_001351095.1:n.24+53_24+58del
NM_001364167.1:c.-126+53_-126+58del	NP_001351096.1:n.-126+53_-126+58del
NR_157093.1:n.301+415_301+420del
NM_000827.4:c.82+415_82+420del MANE Select	NP_000818.2:n.82+415_82+420del
NM_001114183.2:c.82+415_82+420del	NP_001107655.1:n.82+415_82+420del
NM_001258019.2:c.82+415_82+420del	NP_001244948.1:n.82+415_82+420del
NM_001258020.2:c.-261+415_-261+420del	NP_001244949.1:n.-261+415_-261+420del
NM_001364165.2:c.82+415_82+420del	NP_001351094.1:n.82+415_82+420del
NM_001364166.2:c.24+53_24+58del	NP_001351095.1:n.24+53_24+58del
NM_001364167.2:c.-126+53_-126+58del	NP_001351096.1:n.-126+53_-126+58del
NR_047578.2:n.301+415_301+420del
NR_157093.2:n.301+415_301+420del