Canonical Allele Identifier: CA1723285860

Gene: GRM3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86774159A= , CM000669.2:g.86774159A=	GRCh38
NC_000007.13:g.86403475A= , CM000669.1:g.86403475A=	GRCh37
NC_000007.12:g.86241411A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000840.3:c.468+8546A= MANE Select	NP_000831.2:n.468+8546A=
ENST00000361669.7:c.468+8546A= MANE Select	ENSP00000355316.2:n.468+8546A=
NM_000840.2:c.468+8546A=	NP_000831.2:n.468+8546A=
NM_001363522.1:c.468+8546A=	NP_001350451.1:n.468+8546A=
NM_001363522.2:c.468+8546A=	NP_001350451.1:n.468+8546A=
ENST00000361669.6:c.468+8546A=	ENSP00000355316.2:n.468+8546A=
ENST00000439827.1:c.468+8546A=	ENSP00000398767.1:n.468+8546A=
ENST00000454217.1:c.85-12102A=	ENSP00000405427.1:n.85-12102A=
XM_011516088.1:c.468+8546A=	XP_011514390.1:n.468+8546A=
XM_011516089.1:c.468+8546A=	XP_011514391.1:n.468+8546A=
XM_011516090.1:c.468+8546A=	XP_011514392.1:n.468+8546A=
XM_017012073.2:c.468+8546A=	XP_016867562.1:n.468+8546A=
XR_001745256.1:n.5189T=
XR_002956570.1:n.1281T=
XR_002956571.1:n.1279T=
XR_927721.1:n.2616T=