Canonical Allele Identifier: CA595017951

Gene: GRID1

Linked Data

• dbSNP Id: rs1296913110
• gnomAD v2: 10-87608361-AAAC-A
• gnomAD v3: 10-85848604-AAAC-A
• gnomAD v4: 10-85848604-AAAC-A
• MyVariant Identifiers: chr10:g.87608362_87608364del (hg19) ; chr10:g.85848605_85848607del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.85848610_85848612del , CM000672.2:g.85848610_85848612del	GRCh38
NC_000010.10:g.87608367_87608369del , CM000672.1:g.87608367_87608369del	GRCh37
NC_000010.9:g.87598347_87598349del	NCBI36
NG_011875.1:g.522887_522889del

Transcript Alleles

HGVS	Amino-acid change
ENST00000327946.12:c.1233+5889_1233+5891del MANE Select	ENSP00000330148.7:n.1233+5889_1233+5891del
ENST00000327946.11:c.1233+5889_1233+5891del	ENSP00000330148.7:n.1233+5889_1233+5891del
ENST00000464741.2:c.1233+5889_1233+5891del	ENSP00000433064.1:n.1233+5889_1233+5891del
ENST00000536331.5:c.453+5889_453+5891del	ENSP00000444455.2:n.453+5889_453+5891del
NM_017551.2:c.1233+5889_1233+5891del	NP_060021.1:n.1233+5889_1233+5891del
XM_011539720.1:c.1233+5889_1233+5891del	XP_011538022.1:n.1233+5889_1233+5891del
XM_011539720.2:c.1233+5889_1233+5891del	XP_011538022.1:n.1233+5889_1233+5891del
NM_017551.3:c.1233+5889_1233+5891del MANE Select	NP_060021.1:n.1233+5889_1233+5891del