Canonical Allele Identifier: CA930769916
Gene: GRID1 HGNC NCBI

Linked Data

dbSNP Id: rs1842537826
gnomAD v3: 10-85981010-AGCTT-A
gnomAD v4: 10-85981010-AGCTT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85981012_85981015del , CM000672.2:g.85981012_85981015del GRCh38
NC_000010.10:g.87740769_87740772del , CM000672.1:g.87740769_87740772del GRCh37
NC_000010.9:g.87730749_87730752del NCBI36
NG_011875.1:g.390480_390483del

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.727-64775_727-64772del MANE Select ENSP00000330148.7:n.727-64775_727-64772de...
ENST00000327946.11:c.727-64775_727-64772del ENSP00000330148.7:n.727-64775_727-64772de...
ENST00000464741.2:c.727-64775_727-64772del ENSP00000433064.1:n.727-64775_727-64772de...
NM_017551.2:c.727-64775_727-64772del NP_060021.1:n.727-64775_727-64772del
XM_011539720.1:c.727-64775_727-64772del XP_011538022.1:n.727-64775_727-64772del
XM_011539720.2:c.727-64775_727-64772del XP_011538022.1:n.727-64775_727-64772del
NM_017551.3:c.727-64775_727-64772del MANE Select NP_060021.1:n.727-64775_727-64772del
Search 100 bp 5'
Search 100 bp 3'