Canonical Allele Identifier: CA1723318369

Gene: GRM3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86815906T= , CM000669.2:g.86815906T=	GRCh38
NC_000007.13:g.86445222T= , CM000669.1:g.86445222T=	GRCh37
NC_000007.12:g.86283158T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.1325-22933T= MANE Select	ENSP00000355316.2:n.1325-22933T=
ENST00000361669.6:c.1325-22933T=	ENSP00000355316.2:n.1325-22933T=
ENST00000439827.1:c.1324+28790T=	ENSP00000398767.1:n.1324+28790T=
NM_000840.2:c.1325-22933T=	NP_000831.2:n.1325-22933T=
XM_011516088.1:c.1324+28790T=	XP_011514390.1:n.1324+28790T=
XM_011516090.1:c.1325-17116T=	XP_011514392.1:n.1325-17116T=
NM_001363522.1:c.1324+28790T=	NP_001350451.1:n.1324+28790T=
NM_000840.3:c.1325-22933T= MANE Select	NP_000831.2:n.1325-22933T=
NM_001363522.2:c.1324+28790T=	NP_001350451.1:n.1324+28790T=