Canonical Allele Identifier: CA210601559
Gene: GRID1 HGNC NCBI

Linked Data

dbSNP Id: rs1005310309
MyVariant Identifiers: chr10:g.85848717C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85848717C>A , CM000672.2:g.85848717C>A GRCh38
NC_000010.10:g.87608474C>A , CM000672.1:g.87608474C>A GRCh37
NC_000010.9:g.87598454C>A NCBI36
NG_011875.1:g.522777G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327946.12:c.1233+5779G>T MANE Select ENSP00000330148.7:n.1233+5779G>T
ENST00000327946.11:c.1233+5779G>T ENSP00000330148.7:n.1233+5779G>T
ENST00000464741.2:c.1233+5779G>T ENSP00000433064.1:n.1233+5779G>T
ENST00000536331.5:c.453+5779G>T ENSP00000444455.2:n.453+5779G>T
NM_017551.2:c.1233+5779G>T NP_060021.1:n.1233+5779G>T
XM_011539720.1:c.1233+5779G>T XP_011538022.1:n.1233+5779G>T
XM_011539720.2:c.1233+5779G>T XP_011538022.1:n.1233+5779G>T
NM_017551.3:c.1233+5779G>T MANE Select NP_060021.1:n.1233+5779G>T
Search 100 bp 5'
Search 100 bp 3'