Canonical Allele Identifier: CA1925358918
Gene: GRID1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86124406_86124409delinsGACC , CM000672.2:g.86124406_86124409delinsGACC GRCh38
NC_000010.10:g.87884163_87884166delinsGACC , CM000672.1:g.87884163_87884166delinsGACC GRCh37
NC_000010.9:g.87874143_87874146delinsGACC NCBI36
NG_011875.1:g.247085_247088delinsGGTC

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.726+14410_726+14413delinsGGTC MANE Select ENSP00000330148.7:n.726+14410_726+14413de...
ENST00000327946.11:c.726+14410_726+14413delinsGGTC ENSP00000330148.7:n.726+14410_726+14413de...
ENST00000464741.2:c.726+14410_726+14413delinsGGTC ENSP00000433064.1:n.726+14410_726+14413de...
NM_017551.2:c.726+14410_726+14413delinsGGTC NP_060021.1:n.726+14410_726+14413delinsGG...
XM_011539720.1:c.726+14410_726+14413delinsGGTC XP_011538022.1:n.726+14410_726+14413delin...
XM_011539720.2:c.726+14410_726+14413delinsGGTC XP_011538022.1:n.726+14410_726+14413delin...
NM_017551.3:c.726+14410_726+14413delinsGGTC MANE Select NP_060021.1:n.726+14410_726+14413delinsGG...
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