Canonical Allele Identifier: CA1723295392

Gene: GRM3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86786671C= , CM000669.2:g.86786671C=	GRCh38
NC_000007.13:g.86415987C= , CM000669.1:g.86415987C=	GRCh37
NC_000007.12:g.86253923C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.879C= MANE Select	ENSP00000355316.2:p.Ala293=
ENST00000361669.6:c.879C=	ENSP00000355316.2:p.Ala293=
ENST00000439827.1:c.879C=	ENSP00000398767.1:p.Ala293=
ENST00000454217.1:c.495C=	ENSP00000405427.1:p.Ala165=
NM_000840.2:c.879C=	NP_000831.2:p.Ala293=
XM_011516088.1:c.879C=	XP_011514390.1:p.Ala293=
XM_011516089.1:c.879C=	XP_011514391.1:p.Ala293=
XM_011516090.1:c.879C=	XP_011514392.1:p.Ala293=
XR_927721.1:n.1425+6516G=
NM_001363522.1:c.879C=	NP_001350451.1:p.Ala293=
XM_017012073.2:c.879C=	XP_016867562.1:p.Ala293=
XR_002956570.1:n.90+6516G=
XR_002956571.1:n.88+7949G=
NM_000840.3:c.879C= MANE Select	NP_000831.2:p.Ala293=
NM_001363522.2:c.879C=	NP_001350451.1:p.Ala293=