Canonical Allele Identifier: CA1925234083

Gene: GRID1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.85848623_85848625delinsCAG , CM000672.2:g.85848623_85848625delinsCAG	GRCh38
NC_000010.10:g.87608380_87608382delinsCAG , CM000672.1:g.87608380_87608382delinsCAG	GRCh37
NC_000010.9:g.87598360_87598362delinsCAG	NCBI36
NG_011875.1:g.522869_522871delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000327946.12:c.1233+5871_1233+5873delinsCTG MANE Select	ENSP00000330148.7:n.1233+5871_1233+5873delinsCTG
ENST00000327946.11:c.1233+5871_1233+5873delinsCTG	ENSP00000330148.7:n.1233+5871_1233+5873delinsCTG
ENST00000464741.2:c.1233+5871_1233+5873delinsCTG	ENSP00000433064.1:n.1233+5871_1233+5873delinsCTG
ENST00000536331.5:c.453+5871_453+5873delinsCTG	ENSP00000444455.2:n.453+5871_453+5873delinsCTG
NM_017551.2:c.1233+5871_1233+5873delinsCTG	NP_060021.1:n.1233+5871_1233+5873delinsCTG
XM_011539720.1:c.1233+5871_1233+5873delinsCTG	XP_011538022.1:n.1233+5871_1233+5873delinsCTG
XM_011539720.2:c.1233+5871_1233+5873delinsCTG	XP_011538022.1:n.1233+5871_1233+5873delinsCTG
NM_017551.3:c.1233+5871_1233+5873delinsCTG MANE Select	NP_060021.1:n.1233+5871_1233+5873delinsCTG