Canonical Allele Identifier: CA1925234129

Gene: GRID1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.85848697_85848722delinsGTGTTTCCTGAACATTCTACCCTTAA , CM000672.2:g.85848697_85848722delinsGTGTTTCCTGAACATTCTACCCTTAA	GRCh38
NC_000010.10:g.87608454_87608479delinsGTGTTTCCTGAACATTCTACCCTTAA , CM000672.1:g.87608454_87608479delinsGTGTTTCCTGAACATTCTACCCTTAA	GRCh37
NC_000010.9:g.87598434_87598459delinsGTGTTTCCTGAACATTCTACCCTTAA	NCBI36
NG_011875.1:g.522772_522797delinsTTAAGGGTAGAATGTTCAGGAAACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327946.12:c.1233+5774_1233+5799delinsTTAAGGGTAGAATGTTCAGGAAACAC MANE Select	ENSP00000330148.7:n.1233+5774_1233+5799delinsTTAAGGGTAGAATGTT...
ENST00000327946.11:c.1233+5774_1233+5799delinsTTAAGGGTAGAATGTTCAGGAAACAC	ENSP00000330148.7:n.1233+5774_1233+5799delinsTTAAGGGTAGAATGTT...
ENST00000464741.2:c.1233+5774_1233+5799delinsTTAAGGGTAGAATGTTCAGGAAACAC	ENSP00000433064.1:n.1233+5774_1233+5799delinsTTAAGGGTAGAATGTT...
ENST00000536331.5:c.453+5774_453+5799delinsTTAAGGGTAGAATGTTCAGGAAACAC	ENSP00000444455.2:n.453+5774_453+5799delinsTTAAGGGTAGAATGTTCA...
NM_017551.2:c.1233+5774_1233+5799delinsTTAAGGGTAGAATGTTCAGGAAACAC	NP_060021.1:n.1233+5774_1233+5799delinsTTAAGGGTAGAATGTTCAGGAA...
XM_011539720.1:c.1233+5774_1233+5799delinsTTAAGGGTAGAATGTTCAGGAAACAC	XP_011538022.1:n.1233+5774_1233+5799delinsTTAAGGGTAGAATGTTCAG...
XM_011539720.2:c.1233+5774_1233+5799delinsTTAAGGGTAGAATGTTCAGGAAACAC	XP_011538022.1:n.1233+5774_1233+5799delinsTTAAGGGTAGAATGTTCAG...
NM_017551.3:c.1233+5774_1233+5799delinsTTAAGGGTAGAATGTTCAGGAAACAC MANE Select	NP_060021.1:n.1233+5774_1233+5799delinsTTAAGGGTAGAATGTTCAGGAA...