Canonical Allele Identifier: CA2722440370
Gene: GRID1 HGNC NCBI

Linked Data

dbSNP Id: rs2131961739

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86124365_86124367del , CM000672.2:g.86124365_86124367del GRCh38
NC_000010.10:g.87884122_87884124del , CM000672.1:g.87884122_87884124del GRCh37
NC_000010.9:g.87874102_87874104del NCBI36
NG_011875.1:g.247135_247137del

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.726+14460_726+14462del MANE Select ENSP00000330148.7:n.726+14460_726+14462de...
ENST00000327946.11:c.726+14460_726+14462del ENSP00000330148.7:n.726+14460_726+14462de...
ENST00000464741.2:c.726+14460_726+14462del ENSP00000433064.1:n.726+14460_726+14462de...
NM_017551.2:c.726+14460_726+14462del NP_060021.1:n.726+14460_726+14462del
XM_011539720.1:c.726+14460_726+14462del XP_011538022.1:n.726+14460_726+14462del
XM_011539720.2:c.726+14460_726+14462del XP_011538022.1:n.726+14460_726+14462del
NM_017551.3:c.726+14460_726+14462del MANE Select NP_060021.1:n.726+14460_726+14462del