Canonical Allele Identifier: CA1044779472

Gene: GRM7

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.7352646C>A , CM000665.2:g.7352646C>A	GRCh38
NC_000003.11:g.7394333C>A , CM000665.1:g.7394333C>A	GRCh37
NC_000003.10:g.7369333C>A	NCBI36
NG_029781.1:g.496532C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706912.1:c.514+45994C>A	ENSP00000516621.1:n.514+45994C>A
ENST00000357716.9:c.1033+45994C>A MANE Select	ENSP00000350348.4:n.1033+45994C>A
ENST00000357716.8:c.1033+45994C>A	ENSP00000350348.4:n.1033+45994C>A
ENST00000389335.7:c.1033+45994C>A	ENSP00000373986.3:n.1033+45994C>A
ENST00000389336.8:c.1033+45994C>A	ENSP00000373987.4:n.1033+45994C>A
ENST00000402647.6:c.298+45994C>A	ENSP00000384585.4:n.298+45994C>A
ENST00000440923.7:c.1033+45994C>A	ENSP00000412329.3:n.1033+45994C>A
ENST00000461677.6:n.404+45994C>A
ENST00000463676.6:n.298+45994C>A
ENST00000467425.5:c.1033+45994C>A	ENSP00000419835.1:n.1033+45994C>A
ENST00000486284.5:c.1033+45994C>A	ENSP00000417536.1:n.1033+45994C>A
NM_000844.3:c.1033+45994C>A	NP_000835.1:n.1033+45994C>A
NM_181874.2:c.1033+45994C>A	NP_870989.1:n.1033+45994C>A
XR_940422.1:n.1325+45994C>A
XM_017006272.1:c.535+45994C>A	XP_016861761.1:n.535+45994C>A
XM_017006273.1:c.535+45994C>A	XP_016861762.1:n.535+45994C>A
XM_024453492.1:c.-219+45994C>A	XP_024309260.1:n.-219+45994C>A
XM_024453493.1:c.-219+45994C>A	XP_024309261.1:n.-219+45994C>A
XM_024453494.1:c.-219+45994C>A	XP_024309262.1:n.-219+45994C>A
XM_024453495.1:c.-219+45994C>A	XP_024309263.1:n.-219+45994C>A
XM_024453497.1:c.-219+45994C>A	XP_024309265.1:n.-219+45994C>A
XM_024453498.1:c.-219+45994C>A	XP_024309266.1:n.-219+45994C>A
XR_001740134.2:n.1307+45994C>A
XR_001740135.2:n.1307+45994C>A
XR_001740136.2:n.1307+45994C>A
XR_001740137.2:n.1307+45994C>A
NM_000844.4:c.1033+45994C>A MANE Select	NP_000835.1:n.1033+45994C>A
NM_181874.3:c.1033+45994C>A	NP_870989.1:n.1033+45994C>A