Canonical Allele Identifier: CA1925455291
Gene: GRID1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86337967C= , CM000672.2:g.86337967C= GRCh38
NC_000010.10:g.88097724C= , CM000672.1:g.88097724C= GRCh37
NC_000010.9:g.88087704C= NCBI36
NG_011875.1:g.33527G=

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.235+25974G= MANE Select ENSP00000330148.7:n.235+25974G=
ENST00000327946.11:c.235+25974G= ENSP00000330148.7:n.235+25974G=
ENST00000464741.2:c.235+25974G= ENSP00000433064.1:n.235+25974G=
NM_017551.2:c.235+25974G= NP_060021.1:n.235+25974G=
XM_011539720.1:c.235+25974G= XP_011538022.1:n.235+25974G=
XM_011539720.2:c.235+25974G= XP_011538022.1:n.235+25974G=
NM_017551.3:c.235+25974G= MANE Select NP_060021.1:n.235+25974G=
Search 100 bp 5'
Search 100 bp 3'