Canonical Allele Identifier: CA2548471610

Gene: GRIA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.153799363_153799364del , CM000667.2:g.153799363_153799364del	GRCh38
NC_000005.9:g.153178923_153178924del , CM000667.1:g.153178923_153178924del	GRCh37
NC_000005.8:g.153159116_153159117del	NCBI36
NG_047078.1:g.314668_314669del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340592.10:c.2386-2993_2386-2992del	ENSP00000339343.5:n.2386-2993_2386-2992del
ENST00000706733.1:c.2509-2993_2509-2992del	ENSP00000516520.1:n.2509-2993_2509-2992del
ENST00000706734.1:c.2413-2993_2413-2992del	ENSP00000516521.1:n.2413-2993_2413-2992del
ENST00000285900.10:c.2386-2993_2386-2992del MANE Select	ENSP00000285900.4:n.2386-2993_2386-2992del
ENST00000285900.9:c.2386-2993_2386-2992del	ENSP00000285900.4:n.2386-2993_2386-2992del
ENST00000340592.9:c.2386-2993_2386-2992del	ENSP00000339343.5:n.2386-2993_2386-2992del
ENST00000448073.8:c.2416-2993_2416-2992del	ENSP00000415569.2:n.2416-2993_2416-2992del
ENST00000518142.5:c.2146-2993_2146-2992del	ENSP00000427920.1:n.2146-2993_2146-2992del
ENST00000518783.1:c.2416-2993_2416-2992del	ENSP00000428994.1:n.2416-2993_2416-2992del
ENST00000521843.6:c.2179-2993_2179-2992del	ENSP00000427864.2:n.2179-2993_2179-2992del
NM_000827.3:c.2386-2993_2386-2992del	NP_000818.2:n.2386-2993_2386-2992del
NM_001114183.1:c.2386-2993_2386-2992del	NP_001107655.1:n.2386-2993_2386-2992del
NM_001258019.1:c.2146-2993_2146-2992del	NP_001244948.1:n.2146-2993_2146-2992del
NM_001258020.1:c.2101-2993_2101-2992del	NP_001244949.1:n.2101-2993_2101-2992del
NM_001258021.1:c.2416-2993_2416-2992del	NP_001244950.1:n.2416-2993_2416-2992del
NM_001258022.1:c.2416-2993_2416-2992del	NP_001244951.1:n.2416-2993_2416-2992del
NM_001258023.1:c.2179-2993_2179-2992del	NP_001244952.1:n.2179-2993_2179-2992del
NR_047578.1:n.2498-2993_2498-2992del
XM_011537635.1:c.2326-2993_2326-2992del	XP_011535937.1:n.2326-2993_2326-2992del
XR_427776.2:n.2541-2993_2541-2992del
NM_001364165.1:c.2218-2993_2218-2992del	NP_001351094.1:n.2218-2993_2218-2992del
NM_001364166.1:c.2413-2993_2413-2992del	NP_001351095.1:n.2413-2993_2413-2992del
NM_001364167.1:c.2179-2993_2179-2992del	NP_001351096.1:n.2179-2993_2179-2992del
NR_157093.1:n.2720-2993_2720-2992del
XM_017009392.1:c.2426-2993_2426-2992del	XP_016864881.1:n.2426-2993_2426-2992del
NM_000827.4:c.2386-2993_2386-2992del MANE Select	NP_000818.2:n.2386-2993_2386-2992del
NM_001114183.2:c.2386-2993_2386-2992del	NP_001107655.1:n.2386-2993_2386-2992del
NM_001258019.2:c.2146-2993_2146-2992del	NP_001244948.1:n.2146-2993_2146-2992del
NM_001258020.2:c.2101-2993_2101-2992del	NP_001244949.1:n.2101-2993_2101-2992del
NM_001258021.2:c.2416-2993_2416-2992del	NP_001244950.1:n.2416-2993_2416-2992del
NM_001258022.2:c.2416-2993_2416-2992del	NP_001244951.1:n.2416-2993_2416-2992del
NM_001364165.2:c.2218-2993_2218-2992del	NP_001351094.1:n.2218-2993_2218-2992del
NM_001364166.2:c.2413-2993_2413-2992del	NP_001351095.1:n.2413-2993_2413-2992del
NM_001364167.2:c.2179-2993_2179-2992del	NP_001351096.1:n.2179-2993_2179-2992del
NR_047578.2:n.2352-2993_2352-2992del
NR_157093.2:n.2720-2993_2720-2992del