Canonical Allele Identifier: CA210711660

Gene: GRID1

Linked Data

• dbSNP Id: rs143315905
• gnomAD v2: 10-88097717-G-C
• gnomAD v3: 10-86337960-G-C
• gnomAD v4: 10-86337960-G-C
• MyVariant Identifiers: chr10:g.88097717G>C (hg19) ; chr10:g.86337960G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86337960G>C , CM000672.2:g.86337960G>C	GRCh38
NC_000010.10:g.88097717G>C , CM000672.1:g.88097717G>C	GRCh37
NC_000010.9:g.88087697G>C	NCBI36
NG_011875.1:g.33534C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000327946.12:c.235+25981C>G MANE Select	ENSP00000330148.7:n.235+25981C>G
ENST00000327946.11:c.235+25981C>G	ENSP00000330148.7:n.235+25981C>G
ENST00000464741.2:c.235+25981C>G	ENSP00000433064.1:n.235+25981C>G
NM_017551.2:c.235+25981C>G	NP_060021.1:n.235+25981C>G
XM_011539720.1:c.235+25981C>G	XP_011538022.1:n.235+25981C>G
XM_011539720.2:c.235+25981C>G	XP_011538022.1:n.235+25981C>G
NM_017551.3:c.235+25981C>G MANE Select	NP_060021.1:n.235+25981C>G