Canonical Allele Identifier: CA669397444

Gene: GRID1

Linked Data

• dbSNP Id: rs1324240586
• gnomAD v3: 10-85848697-GTGTTTCCTGAACATTCTACCCTTAA-G
• gnomAD v4: 10-85848697-GTGTTTCCTGAACATTCTACCCTTAA-G
• MyVariant Identifiers: chr10:g.87608455_87608479del (hg19) ; chr10:g.85848698_85848722del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.85848700_85848724del , CM000672.2:g.85848700_85848724del	GRCh38
NC_000010.10:g.87608457_87608481del , CM000672.1:g.87608457_87608481del	GRCh37
NC_000010.9:g.87598437_87598461del	NCBI36
NG_011875.1:g.522772_522796del

Transcript Alleles

HGVS	Amino-acid change
ENST00000327946.12:c.1233+5774_1233+5798del MANE Select	ENSP00000330148.7:n.1233+5774_1233+5798del
ENST00000327946.11:c.1233+5774_1233+5798del	ENSP00000330148.7:n.1233+5774_1233+5798del
ENST00000464741.2:c.1233+5774_1233+5798del	ENSP00000433064.1:n.1233+5774_1233+5798del
ENST00000536331.5:c.453+5774_453+5798del	ENSP00000444455.2:n.453+5774_453+5798del
NM_017551.2:c.1233+5774_1233+5798del	NP_060021.1:n.1233+5774_1233+5798del
XM_011539720.1:c.1233+5774_1233+5798del	XP_011538022.1:n.1233+5774_1233+5798del
XM_011539720.2:c.1233+5774_1233+5798del	XP_011538022.1:n.1233+5774_1233+5798del
NM_017551.3:c.1233+5774_1233+5798del MANE Select	NP_060021.1:n.1233+5774_1233+5798del