Canonical Allele Identifier: CA2564356844

Gene: GRIA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.153560978_153560979insGCTT , CM000667.2:g.153560978_153560979insGCTT	GRCh38
NC_000005.9:g.152940538_152940539insGCTT , CM000667.1:g.152940538_152940539insGCTT	GRCh37
NC_000005.8:g.152920731_152920732insGCTT	NCBI36
NG_047078.1:g.76283_76284insGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340592.10:c.220+66913_220+66914insGCTT	ENSP00000339343.5:n.220+66913_220+66914insGCTT
ENST00000520353.6:c.13+66913_13+66914insGCTT	ENSP00000516539.1:n.13+66913_13+66914insGCTT
ENST00000706733.1:c.220+66913_220+66914insGCTT	ENSP00000516520.1:n.220+66913_220+66914insGCTT
ENST00000706734.1:c.247+66913_247+66914insGCTT	ENSP00000516521.1:n.247+66913_247+66914insGCTT
ENST00000706767.1:c.82+70008_82+70009insGCTT	ENSP00000516540.1:n.82+70008_82+70009insGCTT
ENST00000285900.10:c.220+66913_220+66914insGCTT MANE Select	ENSP00000285900.4:n.220+66913_220+66914insGCTT
ENST00000285900.9:c.220+66913_220+66914insGCTT	ENSP00000285900.4:n.220+66913_220+66914insGCTT
ENST00000340592.9:c.220+66913_220+66914insGCTT	ENSP00000339343.5:n.220+66913_220+66914insGCTT
ENST00000448073.8:c.250+66913_250+66914insGCTT	ENSP00000415569.2:n.250+66913_250+66914insGCTT
ENST00000481559.6:n.361+66913_361+66914insGCTT
ENST00000518142.5:c.220+66913_220+66914insGCTT	ENSP00000427920.1:n.220+66913_220+66914insGCTT
ENST00000518783.1:c.250+66913_250+66914insGCTT	ENSP00000428994.1:n.250+66913_250+66914insGCTT
ENST00000518862.5:n.168+66913_168+66914insGCTT
ENST00000521843.6:c.13+66913_13+66914insGCTT	ENSP00000427864.2:n.13+66913_13+66914insGCTT
NM_000827.3:c.220+66913_220+66914insGCTT	NP_000818.2:n.220+66913_220+66914insGCTT
NM_001114183.1:c.220+66913_220+66914insGCTT	NP_001107655.1:n.220+66913_220+66914insGCTT
NM_001258019.1:c.220+66913_220+66914insGCTT	NP_001244948.1:n.220+66913_220+66914insGCTT
NM_001258020.1:c.-66+51172_-66+51173insGCTT	NP_001244949.1:n.-66+51172_-66+51173insGCTT
NM_001258021.1:c.250+66913_250+66914insGCTT	NP_001244950.1:n.250+66913_250+66914insGCTT
NM_001258022.1:c.250+66913_250+66914insGCTT	NP_001244951.1:n.250+66913_250+66914insGCTT
NM_001258023.1:c.13+66913_13+66914insGCTT	NP_001244952.1:n.13+66913_13+66914insGCTT
NR_047578.1:n.447+70008_447+70009insGCTT
XM_011537635.1:c.160+66913_160+66914insGCTT	XP_011535937.1:n.160+66913_160+66914insGCTT
XR_427776.2:n.490+66913_490+66914insGCTT
NM_001364165.1:c.220+66913_220+66914insGCTT	NP_001351094.1:n.220+66913_220+66914insGCTT
NM_001364166.1:c.247+66913_247+66914insGCTT	NP_001351095.1:n.247+66913_247+66914insGCTT
NM_001364167.1:c.13+66913_13+66914insGCTT	NP_001351096.1:n.13+66913_13+66914insGCTT
NR_157093.1:n.439+66913_439+66914insGCTT
XM_017009392.1:c.250+66913_250+66914insGCTT	XP_016864881.1:n.250+66913_250+66914insGCTT
NM_000827.4:c.220+66913_220+66914insGCTT MANE Select	NP_000818.2:n.220+66913_220+66914insGCTT
NM_001114183.2:c.220+66913_220+66914insGCTT	NP_001107655.1:n.220+66913_220+66914insGCTT
NM_001258019.2:c.220+66913_220+66914insGCTT	NP_001244948.1:n.220+66913_220+66914insGCTT
NM_001258020.2:c.-66+51172_-66+51173insGCTT	NP_001244949.1:n.-66+51172_-66+51173insGCTT
NM_001258021.2:c.250+66913_250+66914insGCTT	NP_001244950.1:n.250+66913_250+66914insGCTT
NM_001258022.2:c.250+66913_250+66914insGCTT	NP_001244951.1:n.250+66913_250+66914insGCTT
NM_001364165.2:c.220+66913_220+66914insGCTT	NP_001351094.1:n.220+66913_220+66914insGCTT
NM_001364166.2:c.247+66913_247+66914insGCTT	NP_001351095.1:n.247+66913_247+66914insGCTT
NM_001364167.2:c.13+66913_13+66914insGCTT	NP_001351096.1:n.13+66913_13+66914insGCTT
NR_047578.2:n.301+70008_301+70009insGCTT
NR_157093.2:n.439+66913_439+66914insGCTT