Canonical Allele Identifier: CA210601549

Gene: GRID1

Linked Data

• dbSNP Id: rs141901009
• gnomAD v3: 10-85848623-CAG-C
• gnomAD v4: 10-85848623-CAG-C
• MyVariant Identifiers: chr10:g.87608381_87608382del (hg19) ; chr10:g.85848624_85848625del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.85848625_85848626del , CM000672.2:g.85848625_85848626del	GRCh38
NC_000010.10:g.87608382_87608383del , CM000672.1:g.87608382_87608383del	GRCh37
NC_000010.9:g.87598362_87598363del	NCBI36
NG_011875.1:g.522869_522870del

Transcript Alleles

HGVS	Amino-acid change
ENST00000327946.12:c.1233+5871_1233+5872del MANE Select	ENSP00000330148.7:n.1233+5871_1233+5872del
ENST00000327946.11:c.1233+5871_1233+5872del	ENSP00000330148.7:n.1233+5871_1233+5872del
ENST00000464741.2:c.1233+5871_1233+5872del	ENSP00000433064.1:n.1233+5871_1233+5872del
ENST00000536331.5:c.453+5871_453+5872del	ENSP00000444455.2:n.453+5871_453+5872del
NM_017551.2:c.1233+5871_1233+5872del	NP_060021.1:n.1233+5871_1233+5872del
XM_011539720.1:c.1233+5871_1233+5872del	XP_011538022.1:n.1233+5871_1233+5872del
XM_011539720.2:c.1233+5871_1233+5872del	XP_011538022.1:n.1233+5871_1233+5872del
NM_017551.3:c.1233+5871_1233+5872del MANE Select	NP_060021.1:n.1233+5871_1233+5872del