Canonical Allele Identifier: CA210601564

Gene: GRID1

Linked Data

• dbSNP Id: rs566157930
• gnomAD v2: 10-87608490-T-C
• gnomAD v3: 10-85848733-T-C
• gnomAD v4: 10-85848733-T-C
• MyVariant Identifiers: chr10:g.87608490T>C (hg19) ; chr10:g.85848733T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.85848733T>C , CM000672.2:g.85848733T>C	GRCh38
NC_000010.10:g.87608490T>C , CM000672.1:g.87608490T>C	GRCh37
NC_000010.9:g.87598470T>C	NCBI36
NG_011875.1:g.522761A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000327946.12:c.1233+5763A>G MANE Select	ENSP00000330148.7:n.1233+5763A>G
ENST00000327946.11:c.1233+5763A>G	ENSP00000330148.7:n.1233+5763A>G
ENST00000464741.2:c.1233+5763A>G	ENSP00000433064.1:n.1233+5763A>G
ENST00000536331.5:c.453+5763A>G	ENSP00000444455.2:n.453+5763A>G
NM_017551.2:c.1233+5763A>G	NP_060021.1:n.1233+5763A>G
XM_011539720.1:c.1233+5763A>G	XP_011538022.1:n.1233+5763A>G
XM_011539720.2:c.1233+5763A>G	XP_011538022.1:n.1233+5763A>G
NM_017551.3:c.1233+5763A>G MANE Select	NP_060021.1:n.1233+5763A>G