Canonical Allele Identifier: CA1592494775

Gene: GRIA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.153798953_153798954delinsCG , CM000667.2:g.153798953_153798954delinsCG	GRCh38
NC_000005.9:g.153178513_153178514delinsCG , CM000667.1:g.153178513_153178514delinsCG	GRCh37
NC_000005.8:g.153158706_153158707delinsCG	NCBI36
NG_047078.1:g.314258_314259delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340592.10:c.2385+3363_2385+3364delinsCG	ENSP00000339343.5:n.2385+3363_2385+3364delinsCG
ENST00000706733.1:c.2508+3363_2508+3364delinsCG	ENSP00000516520.1:n.2508+3363_2508+3364delinsCG
ENST00000706734.1:c.2412+3363_2412+3364delinsCG	ENSP00000516521.1:n.2412+3363_2412+3364delinsCG
ENST00000285900.10:c.2386-3403_2386-3402delinsCG MANE Select	ENSP00000285900.4:n.2386-3403_2386-3402delinsCG
ENST00000285900.9:c.2386-3403_2386-3402delinsCG	ENSP00000285900.4:n.2386-3403_2386-3402delinsCG
ENST00000340592.9:c.2385+3363_2385+3364delinsCG	ENSP00000339343.5:n.2385+3363_2385+3364delinsCG
ENST00000448073.8:c.2415+3363_2415+3364delinsCG	ENSP00000415569.2:n.2415+3363_2415+3364delinsCG
ENST00000518142.5:c.2146-3403_2146-3402delinsCG	ENSP00000427920.1:n.2146-3403_2146-3402delinsCG
ENST00000518783.1:c.2416-3403_2416-3402delinsCG	ENSP00000428994.1:n.2416-3403_2416-3402delinsCG
ENST00000521843.6:c.2179-3403_2179-3402delinsCG	ENSP00000427864.2:n.2179-3403_2179-3402delinsCG
NM_000827.3:c.2386-3403_2386-3402delinsCG	NP_000818.2:n.2386-3403_2386-3402delinsCG
NM_001114183.1:c.2385+3363_2385+3364delinsCG	NP_001107655.1:n.2385+3363_2385+3364delinsCG
NM_001258019.1:c.2146-3403_2146-3402delinsCG	NP_001244948.1:n.2146-3403_2146-3402delinsCG
NM_001258020.1:c.2100+3363_2100+3364delinsCG	NP_001244949.1:n.2100+3363_2100+3364delinsCG
NM_001258021.1:c.2416-3403_2416-3402delinsCG	NP_001244950.1:n.2416-3403_2416-3402delinsCG
NM_001258022.1:c.2415+3363_2415+3364delinsCG	NP_001244951.1:n.2415+3363_2415+3364delinsCG
NM_001258023.1:c.2179-3403_2179-3402delinsCG	NP_001244952.1:n.2179-3403_2179-3402delinsCG
NR_047578.1:n.2498-3403_2498-3402delinsCG
XM_011537635.1:c.2325+3363_2325+3364delinsCG	XP_011535937.1:n.2325+3363_2325+3364delinsCG
XR_427776.2:n.2541-3403_2541-3402delinsCG
NM_001364165.1:c.2218-3403_2218-3402delinsCG	NP_001351094.1:n.2218-3403_2218-3402delinsCG
NM_001364166.1:c.2412+3363_2412+3364delinsCG	NP_001351095.1:n.2412+3363_2412+3364delinsCG
NM_001364167.1:c.2178+3363_2178+3364delinsCG	NP_001351096.1:n.2178+3363_2178+3364delinsCG
NR_157093.1:n.2719+3363_2719+3364delinsCG
XM_017009392.1:c.2426-3403_2426-3402delinsCG	XP_016864881.1:n.2426-3403_2426-3402delinsCG
NM_000827.4:c.2386-3403_2386-3402delinsCG MANE Select	NP_000818.2:n.2386-3403_2386-3402delinsCG
NM_001114183.2:c.2385+3363_2385+3364delinsCG	NP_001107655.1:n.2385+3363_2385+3364delinsCG
NM_001258019.2:c.2146-3403_2146-3402delinsCG	NP_001244948.1:n.2146-3403_2146-3402delinsCG
NM_001258020.2:c.2100+3363_2100+3364delinsCG	NP_001244949.1:n.2100+3363_2100+3364delinsCG
NM_001258021.2:c.2416-3403_2416-3402delinsCG	NP_001244950.1:n.2416-3403_2416-3402delinsCG
NM_001258022.2:c.2415+3363_2415+3364delinsCG	NP_001244951.1:n.2415+3363_2415+3364delinsCG
NM_001364165.2:c.2218-3403_2218-3402delinsCG	NP_001351094.1:n.2218-3403_2218-3402delinsCG
NM_001364166.2:c.2412+3363_2412+3364delinsCG	NP_001351095.1:n.2412+3363_2412+3364delinsCG
NM_001364167.2:c.2178+3363_2178+3364delinsCG	NP_001351096.1:n.2178+3363_2178+3364delinsCG
NR_047578.2:n.2352-3403_2352-3402delinsCG
NR_157093.2:n.2719+3363_2719+3364delinsCG