Canonical Allele Identifier: CA1723318254

Gene: GRM3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86815630_86815632delinsCTG , CM000669.2:g.86815630_86815632delinsCTG	GRCh38
NC_000007.13:g.86444946_86444948delinsCTG , CM000669.1:g.86444946_86444948delinsCTG	GRCh37
NC_000007.12:g.86282882_86282884delinsCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361669.7:c.1325-23209_1325-23207delinsCTG MANE Select	ENSP00000355316.2:n.1325-23209_1325-23207...
ENST00000361669.6:c.1325-23209_1325-23207delinsCTG	ENSP00000355316.2:n.1325-23209_1325-23207...
ENST00000439827.1:c.1324+28514_1324+28516delinsCTG	ENSP00000398767.1:n.1324+28514_1324+28516...
NM_000840.2:c.1325-23209_1325-23207delinsCTG	NP_000831.2:n.1325-23209_1325-23207delins...
XM_011516088.1:c.1324+28514_1324+28516delinsCTG	XP_011514390.1:n.1324+28514_1324+28516del...
XM_011516090.1:c.1325-17392_1325-17390delinsCTG	XP_011514392.1:n.1325-17392_1325-17390del...
NM_001363522.1:c.1324+28514_1324+28516delinsCTG	NP_001350451.1:n.1324+28514_1324+28516del...
NM_000840.3:c.1325-23209_1325-23207delinsCTG MANE Select	NP_000831.2:n.1325-23209_1325-23207delins...
NM_001363522.2:c.1324+28514_1324+28516delinsCTG	NP_001350451.1:n.1324+28514_1324+28516del...