Canonical Allele Identifier: CA843335636

Gene: GRM3

Linked Data

• dbSNP Id: rs1450727708
• MyVariant Identifiers: chr7:g.86444864_86444867del (hg19) ; chr7:g.86815548_86815551del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86815551_86815554del , CM000669.2:g.86815551_86815554del	GRCh38
NC_000007.13:g.86444867_86444870del , CM000669.1:g.86444867_86444870del	GRCh37
NC_000007.12:g.86282803_86282806del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.1325-23288_1325-23285del MANE Select	ENSP00000355316.2:n.1325-23288_1325-23285del
ENST00000361669.6:c.1325-23288_1325-23285del	ENSP00000355316.2:n.1325-23288_1325-23285del
ENST00000439827.1:c.1324+28435_1324+28438del	ENSP00000398767.1:n.1324+28435_1324+28438del
NM_000840.2:c.1325-23288_1325-23285del	NP_000831.2:n.1325-23288_1325-23285del
XM_011516088.1:c.1324+28435_1324+28438del	XP_011514390.1:n.1324+28435_1324+28438del
XM_011516090.1:c.1325-17471_1325-17468del	XP_011514392.1:n.1325-17471_1325-17468del
NM_001363522.1:c.1324+28435_1324+28438del	NP_001350451.1:n.1324+28435_1324+28438del
NM_000840.3:c.1325-23288_1325-23285del MANE Select	NP_000831.2:n.1325-23288_1325-23285del
NM_001363522.2:c.1324+28435_1324+28438del	NP_001350451.1:n.1324+28435_1324+28438del