Canonical Allele Identifier: CA1343517002

Gene: GRM7

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.6968394C= , CM000665.2:g.6968394C=	GRCh38
NC_000003.11:g.7010081C= , CM000665.1:g.7010081C=	GRCh37
NC_000003.10:g.6985081C=	NCBI36
NG_029781.1:g.112280C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357716.9:c.519+106487C= MANE Select	ENSP00000350348.4:n.519+106487C=
ENST00000357716.8:c.519+106487C=	ENSP00000350348.4:n.519+106487C=
ENST00000389335.7:c.519+106487C=	ENSP00000373986.3:n.519+106487C=
ENST00000389336.8:c.519+106487C=	ENSP00000373987.4:n.519+106487C=
ENST00000435689.5:c.74+11775C=	ENSP00000405194.1:n.74+11775C=
ENST00000440923.7:c.519+106487C=	ENSP00000412329.3:n.519+106487C=
ENST00000443259.1:c.*115+84088C=	ENSP00000404161.1:n.*115+84088C=
ENST00000448328.6:c.-106+139690C=	ENSP00000393799.2:n.-106+139690C=
ENST00000467425.5:c.519+106487C=	ENSP00000419835.1:n.519+106487C=
ENST00000486284.5:c.519+106487C=	ENSP00000417536.1:n.519+106487C=
NM_000844.3:c.519+106487C=	NP_000835.1:n.519+106487C=
NM_181874.2:c.519+106487C=	NP_870989.1:n.519+106487C=
XR_940422.1:n.811+106487C=
XM_017006272.1:c.21+105393C=	XP_016861761.1:n.21+105393C=
XM_017006273.1:c.21+105393C=	XP_016861762.1:n.21+105393C=
XR_001740134.2:n.793+106487C=
XR_001740135.2:n.793+106487C=
XR_001740136.2:n.793+106487C=
XR_001740137.2:n.793+106487C=
NM_000844.4:c.519+106487C= MANE Select	NP_000835.1:n.519+106487C=
NM_181874.3:c.519+106487C=	NP_870989.1:n.519+106487C=