Canonical Allele Identifier: CA1723318188

Gene: GRM3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86815467T= , CM000669.2:g.86815467T=	GRCh38
NC_000007.13:g.86444783T= , CM000669.1:g.86444783T=	GRCh37
NC_000007.12:g.86282719T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.1325-23372T= MANE Select	ENSP00000355316.2:n.1325-23372T=
ENST00000361669.6:c.1325-23372T=	ENSP00000355316.2:n.1325-23372T=
ENST00000439827.1:c.1324+28351T=	ENSP00000398767.1:n.1324+28351T=
NM_000840.2:c.1325-23372T=	NP_000831.2:n.1325-23372T=
XM_011516088.1:c.1324+28351T=	XP_011514390.1:n.1324+28351T=
XM_011516089.1:c.*220T=	XP_011514391.1:n.*220T=
XM_011516090.1:c.1325-17555T=	XP_011514392.1:n.1325-17555T=
NM_001363522.1:c.1324+28351T=	NP_001350451.1:n.1324+28351T=
NM_000840.3:c.1325-23372T= MANE Select	NP_000831.2:n.1325-23372T=
NM_001363522.2:c.1324+28351T=	NP_001350451.1:n.1324+28351T=