Canonical Allele Identifier: CA1476836319
Gene: GRID2 HGNC NCBI

Linked Data

dbSNP Id: rs1738771954

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.92775949_92775950del , CM000666.2:g.92775949_92775950del GRCh38
NC_000004.11:g.93697100_93697101del , CM000666.1:g.93697100_93697101del GRCh37
NC_000004.10:g.93916123_93916124del NCBI36
NG_034113.1:g.476551_476552del

Transcript Alleles

HGVS Amino-acid change
ENST00000282020.9:c.244+185663_244+185664del MANE Select ENSP00000282020.4:n.244+185663_244+185664...
ENST00000282020.8:c.244+185663_244+185664del ENSP00000282020.4:n.244+185663_244+185664...
ENST00000505687.5:n.416+185663_416+185664del
ENST00000510992.5:c.244+185663_244+185664del ENSP00000421257.1:n.244+185663_244+185664...
NM_001286838.1:c.244+185663_244+185664del NP_001273767.1:n.244+185663_244+185664del...
NM_001510.3:c.244+185663_244+185664del NP_001501.2:n.244+185663_244+185664del
XM_017008122.2:c.244+185663_244+185664del XP_016863611.1:n.244+185663_244+185664del...
XM_024454024.1:c.244+185663_244+185664del XP_024309792.1:n.244+185663_244+185664del...
NM_001510.4:c.244+185663_244+185664del MANE Select NP_001501.2:n.244+185663_244+185664del