Canonical Allele Identifier: CA1925234053
Gene: GRID1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85848559T= , CM000672.2:g.85848559T= GRCh38
NC_000010.10:g.87608316T= , CM000672.1:g.87608316T= GRCh37
NC_000010.9:g.87598296T= NCBI36
NG_011875.1:g.522935A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327946.12:c.1233+5937A= MANE Select ENSP00000330148.7:n.1233+5937A=
ENST00000327946.11:c.1233+5937A= ENSP00000330148.7:n.1233+5937A=
ENST00000464741.2:c.1233+5937A= ENSP00000433064.1:n.1233+5937A=
ENST00000536331.5:c.453+5937A= ENSP00000444455.2:n.453+5937A=
NM_017551.2:c.1233+5937A= NP_060021.1:n.1233+5937A=
XM_011539720.1:c.1233+5937A= XP_011538022.1:n.1233+5937A=
XM_011539720.2:c.1233+5937A= XP_011538022.1:n.1233+5937A=
NM_017551.3:c.1233+5937A= MANE Select NP_060021.1:n.1233+5937A=
Search 100 bp 5'
Search 100 bp 3'