Canonical Allele Identifier: CA1925455287
Gene: GRID1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86337961G= , CM000672.2:g.86337961G= GRCh38
NC_000010.10:g.88097718G= , CM000672.1:g.88097718G= GRCh37
NC_000010.9:g.88087698G= NCBI36
NG_011875.1:g.33533C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327946.12:c.235+25980C= MANE Select ENSP00000330148.7:n.235+25980C=
ENST00000327946.11:c.235+25980C= ENSP00000330148.7:n.235+25980C=
ENST00000464741.2:c.235+25980C= ENSP00000433064.1:n.235+25980C=
NM_017551.2:c.235+25980C= NP_060021.1:n.235+25980C=
XM_011539720.1:c.235+25980C= XP_011538022.1:n.235+25980C=
XM_011539720.2:c.235+25980C= XP_011538022.1:n.235+25980C=
NM_017551.3:c.235+25980C= MANE Select NP_060021.1:n.235+25980C=