Canonical Allele Identifier: CA669397368

Gene: GRID1

Linked Data

• dbSNP Id: rs1404212860
• gnomAD v3: 10-85848525-GT-G
• gnomAD v4: 10-85848525-GT-G
• MyVariant Identifiers: chr10:g.87608283del (hg19) ; chr10:g.85848526del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.85848526del , CM000672.2:g.85848526del	GRCh38
NC_000010.10:g.87608283del , CM000672.1:g.87608283del	GRCh37
NC_000010.9:g.87598263del	NCBI36
NG_011875.1:g.522968del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327946.12:c.1233+5970del MANE Select	ENSP00000330148.7:n.1233+5970del
ENST00000327946.11:c.1233+5970del	ENSP00000330148.7:n.1233+5970del
ENST00000464741.2:c.1233+5970del	ENSP00000433064.1:n.1233+5970del
ENST00000536331.5:c.453+5970del	ENSP00000444455.2:n.453+5970del
NM_017551.2:c.1233+5970del	NP_060021.1:n.1233+5970del
XM_011539720.1:c.1233+5970del	XP_011538022.1:n.1233+5970del
XM_011539720.2:c.1233+5970del	XP_011538022.1:n.1233+5970del
NM_017551.3:c.1233+5970del MANE Select	NP_060021.1:n.1233+5970del