Canonical Allele Identifier: CA210601565
Gene: GRID1 HGNC NCBI

Linked Data

dbSNP Id: rs991709446
MyVariant Identifiers: chr10:g.87608504A>C (hg19) chr10:g.85848747A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85848747A>C , CM000672.2:g.85848747A>C GRCh38
NC_000010.10:g.87608504A>C , CM000672.1:g.87608504A>C GRCh37
NC_000010.9:g.87598484A>C NCBI36
NG_011875.1:g.522747T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.1233+5749T>G MANE Select ENSP00000330148.7:n.1233+5749T>G
ENST00000327946.11:c.1233+5749T>G ENSP00000330148.7:n.1233+5749T>G
ENST00000464741.2:c.1233+5749T>G ENSP00000433064.1:n.1233+5749T>G
ENST00000536331.5:c.453+5749T>G ENSP00000444455.2:n.453+5749T>G
NM_017551.2:c.1233+5749T>G NP_060021.1:n.1233+5749T>G
XM_011539720.1:c.1233+5749T>G XP_011538022.1:n.1233+5749T>G
XM_011539720.2:c.1233+5749T>G XP_011538022.1:n.1233+5749T>G
NM_017551.3:c.1233+5749T>G MANE Select NP_060021.1:n.1233+5749T>G
Search 100 bp 5'
Search 100 bp 3'