Canonical Allele Identifier: CA1723254418

Gene: GRM3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86695998G= , CM000669.2:g.86695998G=	GRCh38
NC_000007.13:g.86325314G= , CM000669.1:g.86325314G=	GRCh37
NC_000007.12:g.86163250G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361669.7:c.-141+51126G= MANE Select	ENSP00000355316.2:n.-141+51126G=
ENST00000361669.6:c.-141+51126G=	ENSP00000355316.2:n.-141+51126G=
ENST00000421579.1:c.-141+51027G=	ENSP00000390037.1:n.-141+51027G=
ENST00000439827.1:c.-141+51126G=	ENSP00000398767.1:n.-141+51126G=
ENST00000454217.1:c.84+51126G=	ENSP00000405427.1:n.84+51126G=
NM_000840.2:c.-141+51126G=	NP_000831.2:n.-141+51126G=
XM_011516088.1:c.-141+51126G=	XP_011514390.1:n.-141+51126G=
XM_011516089.1:c.-141+51126G=	XP_011514391.1:n.-141+51126G=
XM_011516090.1:c.-141+51126G=	XP_011514392.1:n.-141+51126G=
NM_001363522.1:c.-141+51126G=	NP_001350451.1:n.-141+51126G=
XM_017012073.2:c.-141+51126G=	XP_016867562.1:n.-141+51126G=
NM_000840.3:c.-141+51126G= MANE Select	NP_000831.2:n.-141+51126G=
NM_001363522.2:c.-141+51126G=	NP_001350451.1:n.-141+51126G=