Canonical Allele Identifier: CA1925358904
Gene: GRID1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86124381T= , CM000672.2:g.86124381T= GRCh38
NC_000010.10:g.87884138T= , CM000672.1:g.87884138T= GRCh37
NC_000010.9:g.87874118T= NCBI36
NG_011875.1:g.247113A=

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.726+14438A= MANE Select ENSP00000330148.7:n.726+14438A=
ENST00000327946.11:c.726+14438A= ENSP00000330148.7:n.726+14438A=
ENST00000464741.2:c.726+14438A= ENSP00000433064.1:n.726+14438A=
NM_017551.2:c.726+14438A= NP_060021.1:n.726+14438A=
XM_011539720.1:c.726+14438A= XP_011538022.1:n.726+14438A=
XM_011539720.2:c.726+14438A= XP_011538022.1:n.726+14438A=
NM_017551.3:c.726+14438A= MANE Select NP_060021.1:n.726+14438A=
Search 100 bp 5'
Search 100 bp 3'