Canonical Allele Identifier: CA1065449719
Gene: GRID2 HGNC NCBI

Linked Data

dbSNP Id: rs1738771160

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.92775938_92775939del , CM000666.2:g.92775938_92775939del GRCh38
NC_000004.11:g.93697089_93697090del , CM000666.1:g.93697089_93697090del GRCh37
NC_000004.10:g.93916112_93916113del NCBI36
NG_034113.1:g.476540_476541del

Transcript Alleles

HGVS Amino-acid change
ENST00000282020.9:c.244+185652_244+185653del MANE Select ENSP00000282020.4:n.244+185652_244+185653...
ENST00000282020.8:c.244+185652_244+185653del ENSP00000282020.4:n.244+185652_244+185653...
ENST00000505687.5:n.416+185652_416+185653del
ENST00000510992.5:c.244+185652_244+185653del ENSP00000421257.1:n.244+185652_244+185653...
NM_001286838.1:c.244+185652_244+185653del NP_001273767.1:n.244+185652_244+185653del...
NM_001510.3:c.244+185652_244+185653del NP_001501.2:n.244+185652_244+185653del
XM_017008122.2:c.244+185652_244+185653del XP_016863611.1:n.244+185652_244+185653del...
XM_024454024.1:c.244+185652_244+185653del XP_024309792.1:n.244+185652_244+185653del...
NM_001510.4:c.244+185652_244+185653del MANE Select NP_001501.2:n.244+185652_244+185653del