Canonical Allele Identifier: CA800067207

Gene: GRID2

Linked Data

• dbSNP Id: rs1247320496
• gnomAD v3: 4-92775958-TCTG-T
• gnomAD v4: 4-92775958-TCTG-T
• MyVariant Identifiers: chr4:g.93697110_93697112del (hg19) ; chr4:g.92775959_92775961del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.92775960_92775962del , CM000666.2:g.92775960_92775962del	GRCh38
NC_000004.11:g.93697111_93697113del , CM000666.1:g.93697111_93697113del	GRCh37
NC_000004.10:g.93916134_93916136del	NCBI36
NG_034113.1:g.476562_476564del

Transcript Alleles

HGVS	Amino-acid change
ENST00000282020.9:c.244+185674_244+185676del MANE Select	ENSP00000282020.4:n.244+185674_244+185676...
ENST00000282020.8:c.244+185674_244+185676del	ENSP00000282020.4:n.244+185674_244+185676...
ENST00000505687.5:n.416+185674_416+185676del
ENST00000510992.5:c.244+185674_244+185676del	ENSP00000421257.1:n.244+185674_244+185676...
NM_001286838.1:c.244+185674_244+185676del	NP_001273767.1:n.244+185674_244+185676del...
NM_001510.3:c.244+185674_244+185676del	NP_001501.2:n.244+185674_244+185676del
XM_017008122.2:c.244+185674_244+185676del	XP_016863611.1:n.244+185674_244+185676del...
XM_024454024.1:c.244+185674_244+185676del	XP_024309792.1:n.244+185674_244+185676del...
NM_001510.4:c.244+185674_244+185676del MANE Select	NP_001501.2:n.244+185674_244+185676del