Canonical Allele Identifier: CA1989836332

Gene: GRM5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89008492A= , CM000673.2:g.89008492A=	GRCh38
NC_000011.9:g.88741660A= , CM000673.1:g.88741660A=	GRCh37
NC_000011.8:g.88381308A=	NCBI36
NG_052831.1:g.62480T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305447.5:c.661+38720T= MANE Select	ENSP00000306138.4:n.661+38720T=
ENST00000305432.9:c.661+38720T=	ENSP00000305905.5:n.661+38720T=
ENST00000305447.4:c.661+38720T=	ENSP00000306138.4:n.661+38720T=
ENST00000393294.3:c.725+543T=	ENSP00000376972.3:n.725+543T=
ENST00000449371.6:c.223+543T=
ENST00000455756.6:c.661+38720T=	ENSP00000405690.2:n.661+38720T=
NM_000842.4:c.661+38720T=	NP_000833.1:n.661+38720T=
NM_001143831.2:c.661+38720T=	NP_001137303.1:n.661+38720T=
XM_006718828.2:c.661+38720T=	XP_006718891.1:n.661+38720T=
XM_011542792.1:c.661+38720T=	XP_011541094.1:n.661+38720T=
XM_011542793.1:c.661+38720T=	XP_011541095.1:n.661+38720T=
XM_011542794.1:c.661+38720T=	XP_011541096.1:n.661+38720T=
XM_011542795.1:c.661+38720T=	XP_011541097.1:n.661+38720T=
XM_006718828.4:c.661+38720T=	XP_006718891.1:n.661+38720T=
XM_017017627.2:c.661+38720T=	XP_016873116.1:n.661+38720T=
NM_000842.5:c.661+38720T=	NP_000833.1:n.661+38720T=
NM_001143831.3:c.661+38720T= MANE Select	NP_001137303.1:n.661+38720T=
NM_001384268.1:c.661+38720T=	NP_001371197.1:n.661+38720T=