Canonical Allele Identifier: CA1343470444

Gene: GRM7

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.6861610C= , CM000665.2:g.6861610C=	GRCh38
NC_000003.11:g.6903297C= , CM000665.1:g.6903297C=	GRCh37
NC_000003.10:g.6878297C=	NCBI36
NG_029781.1:g.5496C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000844.4:c.222C= MANE Select	NP_000835.1:p.Asn74=
ENST00000357716.9:c.222C= MANE Select	ENSP00000350348.4:p.Asn74=
NM_000844.3:c.222C=	NP_000835.1:p.Asn74=
NM_181874.2:c.222C=	NP_870989.1:p.Asn74=
NM_181874.3:c.222C=	NP_870989.1:p.Asn74=
ENST00000357716.8:c.222C=	ENSP00000350348.4:p.Asn74=
ENST00000389335.7:c.222C=	ENSP00000373986.3:p.Asn74=
ENST00000389336.8:c.222C=	ENSP00000373987.4:p.Asn74=
ENST00000440923.7:c.222C=	ENSP00000412329.3:p.Asn74=
ENST00000443259.1:c.*29-22610C=	ENSP00000404161.1:n.*29-22610C=
ENST00000448328.6:c.-106+32906C=	ENSP00000393799.2:n.-106+32906C=
ENST00000467425.5:c.222C=	ENSP00000419835.1:p.Asn74=
ENST00000486284.5:c.222C=	ENSP00000417536.1:p.Asn74=
XR_001740134.2:n.496C=
XR_001740135.2:n.496C=
XR_001740136.2:n.496C=
XR_001740137.2:n.496C=
XR_940422.1:n.514C=