Canonical Allele Identifier: CA1592494991
Gene: GRIA1 HGNC NCBI

Linked Data

dbSNP Id: rs1765856370

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.153799429_153799436dup , CM000667.2:g.153799429_153799436dup GRCh38
NC_000005.9:g.153178989_153178996dup , CM000667.1:g.153178989_153178996dup GRCh37
NC_000005.8:g.153159182_153159189dup NCBI36
NG_047078.1:g.314734_314741dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000340592.10:c.2386-2927_2386-2920dup ENSP00000339343.5:n.2386-2927_2386-2920dup
ENST00000706733.1:c.2509-2927_2509-2920dup ENSP00000516520.1:n.2509-2927_2509-2920dup
ENST00000706734.1:c.2413-2927_2413-2920dup ENSP00000516521.1:n.2413-2927_2413-2920dup
ENST00000285900.10:c.2386-2927_2386-2920dup MANE Select ENSP00000285900.4:n.2386-2927_2386-2920dup
ENST00000285900.9:c.2386-2927_2386-2920dup ENSP00000285900.4:n.2386-2927_2386-2920dup
ENST00000340592.9:c.2386-2927_2386-2920dup ENSP00000339343.5:n.2386-2927_2386-2920dup
ENST00000448073.8:c.2416-2927_2416-2920dup ENSP00000415569.2:n.2416-2927_2416-2920dup
ENST00000518142.5:c.2146-2927_2146-2920dup ENSP00000427920.1:n.2146-2927_2146-2920dup
ENST00000518783.1:c.2416-2927_2416-2920dup ENSP00000428994.1:n.2416-2927_2416-2920dup
ENST00000521843.6:c.2179-2927_2179-2920dup ENSP00000427864.2:n.2179-2927_2179-2920dup
NM_000827.3:c.2386-2927_2386-2920dup NP_000818.2:n.2386-2927_2386-2920dup
NM_001114183.1:c.2386-2927_2386-2920dup NP_001107655.1:n.2386-2927_2386-2920dup
NM_001258019.1:c.2146-2927_2146-2920dup NP_001244948.1:n.2146-2927_2146-2920dup
NM_001258020.1:c.2101-2927_2101-2920dup NP_001244949.1:n.2101-2927_2101-2920dup
NM_001258021.1:c.2416-2927_2416-2920dup NP_001244950.1:n.2416-2927_2416-2920dup
NM_001258022.1:c.2416-2927_2416-2920dup NP_001244951.1:n.2416-2927_2416-2920dup
NM_001258023.1:c.2179-2927_2179-2920dup NP_001244952.1:n.2179-2927_2179-2920dup
NR_047578.1:n.2498-2927_2498-2920dup
XM_011537635.1:c.2326-2927_2326-2920dup XP_011535937.1:n.2326-2927_2326-2920dup
XR_427776.2:n.2541-2927_2541-2920dup
NM_001364165.1:c.2218-2927_2218-2920dup NP_001351094.1:n.2218-2927_2218-2920dup
NM_001364166.1:c.2413-2927_2413-2920dup NP_001351095.1:n.2413-2927_2413-2920dup
NM_001364167.1:c.2179-2927_2179-2920dup NP_001351096.1:n.2179-2927_2179-2920dup
NR_157093.1:n.2720-2927_2720-2920dup
XM_017009392.1:c.2426-2927_2426-2920dup XP_016864881.1:n.2426-2927_2426-2920dup
NM_000827.4:c.2386-2927_2386-2920dup MANE Select NP_000818.2:n.2386-2927_2386-2920dup
NM_001114183.2:c.2386-2927_2386-2920dup NP_001107655.1:n.2386-2927_2386-2920dup
NM_001258019.2:c.2146-2927_2146-2920dup NP_001244948.1:n.2146-2927_2146-2920dup
NM_001258020.2:c.2101-2927_2101-2920dup NP_001244949.1:n.2101-2927_2101-2920dup
NM_001258021.2:c.2416-2927_2416-2920dup NP_001244950.1:n.2416-2927_2416-2920dup
NM_001258022.2:c.2416-2927_2416-2920dup NP_001244951.1:n.2416-2927_2416-2920dup
NM_001364165.2:c.2218-2927_2218-2920dup NP_001351094.1:n.2218-2927_2218-2920dup
NM_001364166.2:c.2413-2927_2413-2920dup NP_001351095.1:n.2413-2927_2413-2920dup
NM_001364167.2:c.2179-2927_2179-2920dup NP_001351096.1:n.2179-2927_2179-2920dup
NR_047578.2:n.2352-2927_2352-2920dup
NR_157093.2:n.2720-2927_2720-2920dup