Canonical Allele Identifier: CA843335620

Gene: GRM3

Linked Data

• dbSNP Id: rs1380043039
• gnomAD v3: 7-86815493-AAAGT-A
• gnomAD v4: 7-86815493-AAAGT-A
• MyVariant Identifiers: chr7:g.86444810_86444813del (hg19) ; chr7:g.86815494_86815497del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86815497_86815500del , CM000669.2:g.86815497_86815500del	GRCh38
NC_000007.13:g.86444813_86444816del , CM000669.1:g.86444813_86444816del	GRCh37
NC_000007.12:g.86282749_86282752del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.1325-23342_1325-23339del MANE Select	ENSP00000355316.2:n.1325-23342_1325-23339del
ENST00000361669.6:c.1325-23342_1325-23339del	ENSP00000355316.2:n.1325-23342_1325-23339del
ENST00000439827.1:c.1324+28381_1324+28384del	ENSP00000398767.1:n.1324+28381_1324+28384del
NM_000840.2:c.1325-23342_1325-23339del	NP_000831.2:n.1325-23342_1325-23339del
XM_011516088.1:c.1324+28381_1324+28384del	XP_011514390.1:n.1324+28381_1324+28384del
XM_011516090.1:c.1325-17525_1325-17522del	XP_011514392.1:n.1325-17525_1325-17522del
NM_001363522.1:c.1324+28381_1324+28384del	NP_001350451.1:n.1324+28381_1324+28384del
NM_000840.3:c.1325-23342_1325-23339del MANE Select	NP_000831.2:n.1325-23342_1325-23339del
NM_001363522.2:c.1324+28381_1324+28384del	NP_001350451.1:n.1324+28381_1324+28384del