Canonical Allele Identifier: CA1925234075

Gene: GRID1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.85848604_85848607delinsAAAC , CM000672.2:g.85848604_85848607delinsAAAC	GRCh38
NC_000010.10:g.87608361_87608364delinsAAAC , CM000672.1:g.87608361_87608364delinsAAAC	GRCh37
NC_000010.9:g.87598341_87598344delinsAAAC	NCBI36
NG_011875.1:g.522887_522890delinsGTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000327946.12:c.1233+5889_1233+5892delinsGTTT MANE Select	ENSP00000330148.7:n.1233+5889_1233+5892delinsGTTT
ENST00000327946.11:c.1233+5889_1233+5892delinsGTTT	ENSP00000330148.7:n.1233+5889_1233+5892delinsGTTT
ENST00000464741.2:c.1233+5889_1233+5892delinsGTTT	ENSP00000433064.1:n.1233+5889_1233+5892delinsGTTT
ENST00000536331.5:c.453+5889_453+5892delinsGTTT	ENSP00000444455.2:n.453+5889_453+5892delinsGTTT
NM_017551.2:c.1233+5889_1233+5892delinsGTTT	NP_060021.1:n.1233+5889_1233+5892delinsGTTT
XM_011539720.1:c.1233+5889_1233+5892delinsGTTT	XP_011538022.1:n.1233+5889_1233+5892delinsGTTT
XM_011539720.2:c.1233+5889_1233+5892delinsGTTT	XP_011538022.1:n.1233+5889_1233+5892delinsGTTT
NM_017551.3:c.1233+5889_1233+5892delinsGTTT MANE Select	NP_060021.1:n.1233+5889_1233+5892delinsGTTT