Canonical Allele Identifier: CA1083096896

Gene: GRIA1

Linked Data

• gnomAD v3: 5-153560976-G-GTGGTCGCCGT
• gnomAD v4: 5-153560976-G-GTGGTCGCCGT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.153560976_153560977insTGGTCGCCGT , CM000667.2:g.153560976_153560977insTGGTCGCCGT	GRCh38
NC_000005.9:g.152940536_152940537insTGGTCGCCGT , CM000667.1:g.152940536_152940537insTGGTCGCCGT	GRCh37
NC_000005.8:g.152920729_152920730insTGGTCGCCGT	NCBI36
NG_047078.1:g.76281_76282insTGGTCGCCGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340592.10:c.220+66911_220+66912insTGGTCGCCGT	ENSP00000339343.5:n.220+66911_220+66912insTGGTCGCCGT
ENST00000520353.6:c.13+66911_13+66912insTGGTCGCCGT	ENSP00000516539.1:n.13+66911_13+66912insTGGTCGCCGT
ENST00000706733.1:c.220+66911_220+66912insTGGTCGCCGT	ENSP00000516520.1:n.220+66911_220+66912insTGGTCGCCGT
ENST00000706734.1:c.247+66911_247+66912insTGGTCGCCGT	ENSP00000516521.1:n.247+66911_247+66912insTGGTCGCCGT
ENST00000706767.1:c.82+70006_82+70007insTGGTCGCCGT	ENSP00000516540.1:n.82+70006_82+70007insTGGTCGCCGT
ENST00000285900.10:c.220+66911_220+66912insTGGTCGCCGT MANE Select	ENSP00000285900.4:n.220+66911_220+66912insTGGTCGCCGT
ENST00000285900.9:c.220+66911_220+66912insTGGTCGCCGT	ENSP00000285900.4:n.220+66911_220+66912insTGGTCGCCGT
ENST00000340592.9:c.220+66911_220+66912insTGGTCGCCGT	ENSP00000339343.5:n.220+66911_220+66912insTGGTCGCCGT
ENST00000448073.8:c.250+66911_250+66912insTGGTCGCCGT	ENSP00000415569.2:n.250+66911_250+66912insTGGTCGCCGT
ENST00000481559.6:n.361+66911_361+66912insTGGTCGCCGT
ENST00000518142.5:c.220+66911_220+66912insTGGTCGCCGT	ENSP00000427920.1:n.220+66911_220+66912insTGGTCGCCGT
ENST00000518783.1:c.250+66911_250+66912insTGGTCGCCGT	ENSP00000428994.1:n.250+66911_250+66912insTGGTCGCCGT
ENST00000518862.5:n.168+66911_168+66912insTGGTCGCCGT
ENST00000521843.6:c.13+66911_13+66912insTGGTCGCCGT	ENSP00000427864.2:n.13+66911_13+66912insTGGTCGCCGT
NM_000827.3:c.220+66911_220+66912insTGGTCGCCGT	NP_000818.2:n.220+66911_220+66912insTGGTCGCCGT
NM_001114183.1:c.220+66911_220+66912insTGGTCGCCGT	NP_001107655.1:n.220+66911_220+66912insTGGTCGCCGT
NM_001258019.1:c.220+66911_220+66912insTGGTCGCCGT	NP_001244948.1:n.220+66911_220+66912insTGGTCGCCGT
NM_001258020.1:c.-66+51170_-66+51171insTGGTCGCCGT	NP_001244949.1:n.-66+51170_-66+51171insTGGTCGCCGT
NM_001258021.1:c.250+66911_250+66912insTGGTCGCCGT	NP_001244950.1:n.250+66911_250+66912insTGGTCGCCGT
NM_001258022.1:c.250+66911_250+66912insTGGTCGCCGT	NP_001244951.1:n.250+66911_250+66912insTGGTCGCCGT
NM_001258023.1:c.13+66911_13+66912insTGGTCGCCGT	NP_001244952.1:n.13+66911_13+66912insTGGTCGCCGT
NR_047578.1:n.447+70006_447+70007insTGGTCGCCGT
XM_011537635.1:c.160+66911_160+66912insTGGTCGCCGT	XP_011535937.1:n.160+66911_160+66912insTGGTCGCCGT
XR_427776.2:n.490+66911_490+66912insTGGTCGCCGT
NM_001364165.1:c.220+66911_220+66912insTGGTCGCCGT	NP_001351094.1:n.220+66911_220+66912insTGGTCGCCGT
NM_001364166.1:c.247+66911_247+66912insTGGTCGCCGT	NP_001351095.1:n.247+66911_247+66912insTGGTCGCCGT
NM_001364167.1:c.13+66911_13+66912insTGGTCGCCGT	NP_001351096.1:n.13+66911_13+66912insTGGTCGCCGT
NR_157093.1:n.439+66911_439+66912insTGGTCGCCGT
XM_017009392.1:c.250+66911_250+66912insTGGTCGCCGT	XP_016864881.1:n.250+66911_250+66912insTGGTCGCCGT
NM_000827.4:c.220+66911_220+66912insTGGTCGCCGT MANE Select	NP_000818.2:n.220+66911_220+66912insTGGTCGCCGT
NM_001114183.2:c.220+66911_220+66912insTGGTCGCCGT	NP_001107655.1:n.220+66911_220+66912insTGGTCGCCGT
NM_001258019.2:c.220+66911_220+66912insTGGTCGCCGT	NP_001244948.1:n.220+66911_220+66912insTGGTCGCCGT
NM_001258020.2:c.-66+51170_-66+51171insTGGTCGCCGT	NP_001244949.1:n.-66+51170_-66+51171insTGGTCGCCGT
NM_001258021.2:c.250+66911_250+66912insTGGTCGCCGT	NP_001244950.1:n.250+66911_250+66912insTGGTCGCCGT
NM_001258022.2:c.250+66911_250+66912insTGGTCGCCGT	NP_001244951.1:n.250+66911_250+66912insTGGTCGCCGT
NM_001364165.2:c.220+66911_220+66912insTGGTCGCCGT	NP_001351094.1:n.220+66911_220+66912insTGGTCGCCGT
NM_001364166.2:c.247+66911_247+66912insTGGTCGCCGT	NP_001351095.1:n.247+66911_247+66912insTGGTCGCCGT
NM_001364167.2:c.13+66911_13+66912insTGGTCGCCGT	NP_001351096.1:n.13+66911_13+66912insTGGTCGCCGT
NR_047578.2:n.301+70006_301+70007insTGGTCGCCGT
NR_157093.2:n.439+66911_439+66912insTGGTCGCCGT