Canonical Allele Identifier: CA1925455283

Gene: GRID1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86337959_86337960delinsCG , CM000672.2:g.86337959_86337960delinsCG	GRCh38
NC_000010.10:g.88097716_88097717delinsCG , CM000672.1:g.88097716_88097717delinsCG	GRCh37
NC_000010.9:g.88087696_88087697delinsCG	NCBI36
NG_011875.1:g.33534_33535delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000327946.12:c.235+25981_235+25982delinsCG MANE Select	ENSP00000330148.7:n.235+25981_235+25982delinsCG
ENST00000327946.11:c.235+25981_235+25982delinsCG	ENSP00000330148.7:n.235+25981_235+25982delinsCG
ENST00000464741.2:c.235+25981_235+25982delinsCG	ENSP00000433064.1:n.235+25981_235+25982delinsCG
NM_017551.2:c.235+25981_235+25982delinsCG	NP_060021.1:n.235+25981_235+25982delinsCG
XM_011539720.1:c.235+25981_235+25982delinsCG	XP_011538022.1:n.235+25981_235+25982delinsCG
XM_011539720.2:c.235+25981_235+25982delinsCG	XP_011538022.1:n.235+25981_235+25982delinsCG
NM_017551.3:c.235+25981_235+25982delinsCG MANE Select	NP_060021.1:n.235+25981_235+25982delinsCG