Canonical Allele Identifier: CA1723298088

Gene: GRM3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86792916T>A , CM000669.2:g.86792916T>A	GRCh38
NC_000007.13:g.86422232T>A , CM000669.1:g.86422232T>A	GRCh37
NC_000007.12:g.86260168T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.1324+5800T>A MANE Select	ENSP00000355316.2:n.1324+5800T>A
ENST00000361669.6:c.1324+5800T>A	ENSP00000355316.2:n.1324+5800T>A
ENST00000439827.1:c.1324+5800T>A	ENSP00000398767.1:n.1324+5800T>A
NM_000840.2:c.1324+5800T>A	NP_000831.2:n.1324+5800T>A
XM_011516088.1:c.1324+5800T>A	XP_011514390.1:n.1324+5800T>A
XM_011516089.1:c.1324+5800T>A	XP_011514391.1:n.1324+5800T>A
XM_011516090.1:c.1324+5800T>A	XP_011514392.1:n.1324+5800T>A
XR_927721.1:n.1425+271A>T
NM_001363522.1:c.1324+5800T>A	NP_001350451.1:n.1324+5800T>A
XM_017012073.2:c.1325-132T>A	XP_016867562.1:n.1325-132T>A
XR_002956570.1:n.90+271A>T
XR_002956571.1:n.88+1704A>T
NM_000840.3:c.1324+5800T>A MANE Select	NP_000831.2:n.1324+5800T>A
NM_001363522.2:c.1324+5800T>A	NP_001350451.1:n.1324+5800T>A