Canonical Allele Identifier: CA2768977390

Gene: GRIA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.153799338_153799339insAG , CM000667.2:g.153799338_153799339insAG	GRCh38
NC_000005.9:g.153178898_153178899insAG , CM000667.1:g.153178898_153178899insAG	GRCh37
NC_000005.8:g.153159091_153159092insAG	NCBI36
NG_047078.1:g.314643_314644insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340592.10:c.2386-3018_2386-3017insAG	ENSP00000339343.5:n.2386-3018_2386-3017insAG
ENST00000706733.1:c.2509-3018_2509-3017insAG	ENSP00000516520.1:n.2509-3018_2509-3017insAG
ENST00000706734.1:c.2413-3018_2413-3017insAG	ENSP00000516521.1:n.2413-3018_2413-3017insAG
ENST00000285900.10:c.2386-3018_2386-3017insAG MANE Select	ENSP00000285900.4:n.2386-3018_2386-3017insAG
ENST00000285900.9:c.2386-3018_2386-3017insAG	ENSP00000285900.4:n.2386-3018_2386-3017insAG
ENST00000340592.9:c.2386-3018_2386-3017insAG	ENSP00000339343.5:n.2386-3018_2386-3017insAG
ENST00000448073.8:c.2416-3018_2416-3017insAG	ENSP00000415569.2:n.2416-3018_2416-3017insAG
ENST00000518142.5:c.2146-3018_2146-3017insAG	ENSP00000427920.1:n.2146-3018_2146-3017insAG
ENST00000518783.1:c.2416-3018_2416-3017insAG	ENSP00000428994.1:n.2416-3018_2416-3017insAG
ENST00000521843.6:c.2179-3018_2179-3017insAG	ENSP00000427864.2:n.2179-3018_2179-3017insAG
NM_000827.3:c.2386-3018_2386-3017insAG	NP_000818.2:n.2386-3018_2386-3017insAG
NM_001114183.1:c.2386-3018_2386-3017insAG	NP_001107655.1:n.2386-3018_2386-3017insAG
NM_001258019.1:c.2146-3018_2146-3017insAG	NP_001244948.1:n.2146-3018_2146-3017insAG
NM_001258020.1:c.2101-3018_2101-3017insAG	NP_001244949.1:n.2101-3018_2101-3017insAG
NM_001258021.1:c.2416-3018_2416-3017insAG	NP_001244950.1:n.2416-3018_2416-3017insAG
NM_001258022.1:c.2416-3018_2416-3017insAG	NP_001244951.1:n.2416-3018_2416-3017insAG
NM_001258023.1:c.2179-3018_2179-3017insAG	NP_001244952.1:n.2179-3018_2179-3017insAG
NR_047578.1:n.2498-3018_2498-3017insAG
XM_011537635.1:c.2326-3018_2326-3017insAG	XP_011535937.1:n.2326-3018_2326-3017insAG
XR_427776.2:n.2541-3018_2541-3017insAG
NM_001364165.1:c.2218-3018_2218-3017insAG	NP_001351094.1:n.2218-3018_2218-3017insAG
NM_001364166.1:c.2413-3018_2413-3017insAG	NP_001351095.1:n.2413-3018_2413-3017insAG
NM_001364167.1:c.2179-3018_2179-3017insAG	NP_001351096.1:n.2179-3018_2179-3017insAG
NR_157093.1:n.2720-3018_2720-3017insAG
XM_017009392.1:c.2426-3018_2426-3017insAG	XP_016864881.1:n.2426-3018_2426-3017insAG
NM_000827.4:c.2386-3018_2386-3017insAG MANE Select	NP_000818.2:n.2386-3018_2386-3017insAG
NM_001114183.2:c.2386-3018_2386-3017insAG	NP_001107655.1:n.2386-3018_2386-3017insAG
NM_001258019.2:c.2146-3018_2146-3017insAG	NP_001244948.1:n.2146-3018_2146-3017insAG
NM_001258020.2:c.2101-3018_2101-3017insAG	NP_001244949.1:n.2101-3018_2101-3017insAG
NM_001258021.2:c.2416-3018_2416-3017insAG	NP_001244950.1:n.2416-3018_2416-3017insAG
NM_001258022.2:c.2416-3018_2416-3017insAG	NP_001244951.1:n.2416-3018_2416-3017insAG
NM_001364165.2:c.2218-3018_2218-3017insAG	NP_001351094.1:n.2218-3018_2218-3017insAG
NM_001364166.2:c.2413-3018_2413-3017insAG	NP_001351095.1:n.2413-3018_2413-3017insAG
NM_001364167.2:c.2179-3018_2179-3017insAG	NP_001351096.1:n.2179-3018_2179-3017insAG
NR_047578.2:n.2352-3018_2352-3017insAG
NR_157093.2:n.2720-3018_2720-3017insAG