Canonical Allele Identifier: CA362001630
Community Standard Title: NM_000827.4(GRIA1):c.2392A>G (p.Thr798Ala)
Gene: GRIA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.153802362A>G , CM000667.2:g.153802362A>G GRCh38
NC_000005.9:g.153181922A>G , CM000667.1:g.153181922A>G GRCh37
NC_000005.8:g.153162115A>G NCBI36
NG_047078.1:g.317667A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000827.4:c.2392A>G MANE Select NP_000818.2:p.Thr798Ala
ENST00000285900.10:c.2392A>G MANE Select ENSP00000285900.4:p.Thr798Ala
NM_000827.3:c.2392A>G NP_000818.2:p.Thr798Ala
NM_001114183.1:c.2392A>G NP_001107655.1:p.Thr798Ala
NM_001114183.2:c.2392A>G NP_001107655.1:p.Thr798Ala
NM_001258019.1:c.2152A>G NP_001244948.1:p.Thr718Ala
NM_001258019.2:c.2152A>G NP_001244948.1:p.Thr718Ala
NM_001258020.1:c.2107A>G NP_001244949.1:p.Thr703Ala
NM_001258020.2:c.2107A>G NP_001244949.1:p.Thr703Ala
NM_001258021.1:c.2422A>G NP_001244950.1:p.Thr808Ala
NM_001258021.2:c.2422A>G NP_001244950.1:p.Thr808Ala
NM_001258022.1:c.2422A>G NP_001244951.1:p.Thr808Ala
NM_001258022.2:c.2422A>G NP_001244951.1:p.Thr808Ala
NM_001258023.1:c.2185A>G NP_001244952.1:p.Thr729Ala
NM_001364165.1:c.2224A>G NP_001351094.1:p.Thr742Ala
NM_001364165.2:c.2224A>G NP_001351094.1:p.Thr742Ala
NM_001364166.1:c.2419A>G NP_001351095.1:p.Thr807Ala
NM_001364166.2:c.2419A>G NP_001351095.1:p.Thr807Ala
NM_001364167.1:c.2185A>G NP_001351096.1:p.Thr729Ala
NM_001364167.2:c.2185A>G NP_001351096.1:p.Thr729Ala
NR_047578.1:n.2504A>G
NR_047578.2:n.2358A>G
NR_157093.1:n.2726A>G
NR_157093.2:n.2726A>G
ENST00000285900.9:c.2392A>G ENSP00000285900.4:p.Thr798Ala
ENST00000340592.10:c.2392A>G ENSP00000339343.5:p.Thr798Ala
ENST00000340592.9:c.2392A>G ENSP00000339343.5:p.Thr798Ala
ENST00000448073.8:c.2422A>G ENSP00000415569.2:p.Thr808Ala
ENST00000518142.5:c.2152A>G ENSP00000427920.1:p.Thr718Ala
ENST00000518783.1:c.2422A>G ENSP00000428994.1:p.Thr808Ala
ENST00000521843.6:c.2185A>G ENSP00000427864.2:p.Thr729Ala
ENST00000706733.1:c.2515A>G ENSP00000516520.1:p.Thr839Ala
ENST00000706734.1:c.2419A>G ENSP00000516521.1:p.Thr807Ala
XM_011537635.1:c.2332A>G XP_011535937.1:p.Thr778Ala
XM_017009392.1:c.2432A>G XP_016864881.1:p.Asp811Gly
XR_427776.2:n.2547A>G