Canonical Allele Identifier: CA909948597

Gene: GRM7

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.7114015T>G , CM000665.2:g.7114015T>G	GRCh38
NC_000003.11:g.7155702T>G , CM000665.1:g.7155702T>G	GRCh37
NC_000003.10:g.7130702T>G	NCBI36
NG_029781.1:g.257901T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357716.9:c.520-32437T>G MANE Select	ENSP00000350348.4:n.520-32437T>G
ENST00000357716.8:c.520-32437T>G	ENSP00000350348.4:n.520-32437T>G
ENST00000389335.7:c.520-32437T>G	ENSP00000373986.3:n.520-32437T>G
ENST00000389336.8:c.520-32437T>G	ENSP00000373987.4:n.520-32437T>G
ENST00000435689.5:c.75-32437T>G	ENSP00000405194.1:n.75-32437T>G
ENST00000440923.7:c.520-32437T>G	ENSP00000412329.3:n.520-32437T>G
ENST00000443259.1:c.*116-32437T>G	ENSP00000404161.1:n.*116-32437T>G
ENST00000448328.6:c.-105-32437T>G	ENSP00000393799.2:n.-105-32437T>G
ENST00000467425.5:c.520-32437T>G	ENSP00000419835.1:n.520-32437T>G
ENST00000486284.5:c.520-32437T>G	ENSP00000417536.1:n.520-32437T>G
NM_000844.3:c.520-32437T>G	NP_000835.1:n.520-32437T>G
NM_181874.2:c.520-32437T>G	NP_870989.1:n.520-32437T>G
XR_940422.1:n.812-32437T>G
XM_017006272.1:c.22-32437T>G	XP_016861761.1:n.22-32437T>G
XM_017006273.1:c.22-32437T>G	XP_016861762.1:n.22-32437T>G
XR_001740134.2:n.794-32437T>G
XR_001740135.2:n.794-32437T>G
XR_001740136.2:n.794-32437T>G
XR_001740137.2:n.794-32437T>G
NM_000844.4:c.520-32437T>G MANE Select	NP_000835.1:n.520-32437T>G
NM_181874.3:c.520-32437T>G	NP_870989.1:n.520-32437T>G