Canonical Allele Identifier: CA1723297260

Gene: GRM3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86791061T= , CM000669.2:g.86791061T=	GRCh38
NC_000007.13:g.86420377T= , CM000669.1:g.86420377T=	GRCh37
NC_000007.12:g.86258313T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000840.3:c.1324+3945T= MANE Select	NP_000831.2:n.1324+3945T=
ENST00000361669.7:c.1324+3945T= MANE Select	ENSP00000355316.2:n.1324+3945T=
NM_000840.2:c.1324+3945T=	NP_000831.2:n.1324+3945T=
NM_001363522.1:c.1324+3945T=	NP_001350451.1:n.1324+3945T=
NM_001363522.2:c.1324+3945T=	NP_001350451.1:n.1324+3945T=
ENST00000361669.6:c.1324+3945T=	ENSP00000355316.2:n.1324+3945T=
ENST00000439827.1:c.1324+3945T=	ENSP00000398767.1:n.1324+3945T=
XM_011516088.1:c.1324+3945T=	XP_011514390.1:n.1324+3945T=
XM_011516089.1:c.1324+3945T=	XP_011514391.1:n.1324+3945T=
XM_011516090.1:c.1324+3945T=	XP_011514392.1:n.1324+3945T=
XM_017012073.2:c.1325-1987T=	XP_016867562.1:n.1325-1987T=
XR_002956570.1:n.90+2126A=
XR_002956571.1:n.88+3559A=
XR_927721.1:n.1425+2126A=