Canonical Allele Identifier: CA2234591

Gene: GRM7

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.6861914A>G , CM000665.2:g.6861914A>G	GRCh38
NC_000003.11:g.6903601A>G , CM000665.1:g.6903601A>G	GRCh37
NC_000003.10:g.6878601A>G	NCBI36
NG_029781.1:g.5800A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000844.4:c.519+7A>G MANE Select	NP_000835.1:n.519+7A>G
ENST00000357716.9:c.519+7A>G MANE Select	ENSP00000350348.4:n.519+7A>G
NM_000844.3:c.519+7A>G	NP_000835.1:n.519+7A>G
NM_181874.2:c.519+7A>G	NP_870989.1:n.519+7A>G
NM_181874.3:c.519+7A>G	NP_870989.1:n.519+7A>G
ENST00000357716.8:c.519+7A>G	ENSP00000350348.4:n.519+7A>G
ENST00000389335.7:c.519+7A>G	ENSP00000373986.3:n.519+7A>G
ENST00000389336.8:c.519+7A>G	ENSP00000373987.4:n.519+7A>G
ENST00000440923.7:c.519+7A>G	ENSP00000412329.3:n.519+7A>G
ENST00000443259.1:c.*29-22306A>G	ENSP00000404161.1:n.*29-22306A>G
ENST00000448328.6:c.-106+33210A>G	ENSP00000393799.2:n.-106+33210A>G
ENST00000467425.5:c.519+7A>G	ENSP00000419835.1:n.519+7A>G
ENST00000486284.5:c.519+7A>G	ENSP00000417536.1:n.519+7A>G
XR_001740134.2:n.793+7A>G
XR_001740135.2:n.793+7A>G
XR_001740136.2:n.793+7A>G
XR_001740137.2:n.793+7A>G
XR_940422.1:n.811+7A>G