Canonical Allele Identifier: CA930772341
Gene: GRID1 HGNC NCBI

Linked Data

dbSNP Id: rs1844719718
gnomAD v3: 10-86124288-TTGA-T
gnomAD v4: 10-86124288-TTGA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86124290_86124292del , CM000672.2:g.86124290_86124292del GRCh38
NC_000010.10:g.87884047_87884049del , CM000672.1:g.87884047_87884049del GRCh37
NC_000010.9:g.87874027_87874029del NCBI36
NG_011875.1:g.247203_247205del

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.726+14528_726+14530del MANE Select ENSP00000330148.7:n.726+14528_726+14530de...
ENST00000327946.11:c.726+14528_726+14530del ENSP00000330148.7:n.726+14528_726+14530de...
ENST00000464741.2:c.726+14528_726+14530del ENSP00000433064.1:n.726+14528_726+14530de...
NM_017551.2:c.726+14528_726+14530del NP_060021.1:n.726+14528_726+14530del
XM_011539720.1:c.726+14528_726+14530del XP_011538022.1:n.726+14528_726+14530del
XM_011539720.2:c.726+14528_726+14530del XP_011538022.1:n.726+14528_726+14530del
NM_017551.3:c.726+14528_726+14530del MANE Select NP_060021.1:n.726+14528_726+14530del
Search 100 bp 5'
Search 100 bp 3'