Canonical Allele Identifier: CA1925358849
Gene: GRID1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86124288_86124291delinsTTGA , CM000672.2:g.86124288_86124291delinsTTGA GRCh38
NC_000010.10:g.87884045_87884048delinsTTGA , CM000672.1:g.87884045_87884048delinsTTGA GRCh37
NC_000010.9:g.87874025_87874028delinsTTGA NCBI36
NG_011875.1:g.247203_247206delinsTCAA

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.726+14528_726+14531delinsTCAA MANE Select ENSP00000330148.7:n.726+14528_726+14531de...
ENST00000327946.11:c.726+14528_726+14531delinsTCAA ENSP00000330148.7:n.726+14528_726+14531de...
ENST00000464741.2:c.726+14528_726+14531delinsTCAA ENSP00000433064.1:n.726+14528_726+14531de...
NM_017551.2:c.726+14528_726+14531delinsTCAA NP_060021.1:n.726+14528_726+14531delinsTC...
XM_011539720.1:c.726+14528_726+14531delinsTCAA XP_011538022.1:n.726+14528_726+14531delin...
XM_011539720.2:c.726+14528_726+14531delinsTCAA XP_011538022.1:n.726+14528_726+14531delin...
NM_017551.3:c.726+14528_726+14531delinsTCAA MANE Select NP_060021.1:n.726+14528_726+14531delinsTC...
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