Canonical Allele Identifier: CA15531770

Gene: GRM3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86702440T>C , CM000669.2:g.86702440T>C	GRCh38
NC_000007.13:g.86331756T>C , CM000669.1:g.86331756T>C	GRCh37
NC_000007.12:g.86169692T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.-141+57568T>C MANE Select	ENSP00000355316.2:n.-141+57568T>C
ENST00000361669.6:c.-141+57568T>C	ENSP00000355316.2:n.-141+57568T>C
ENST00000421579.1:c.-141+57469T>C	ENSP00000390037.1:n.-141+57469T>C
ENST00000439827.1:c.-141+57568T>C	ENSP00000398767.1:n.-141+57568T>C
ENST00000454217.1:c.84+57568T>C	ENSP00000405427.1:n.84+57568T>C
NM_000840.2:c.-141+57568T>C	NP_000831.2:n.-141+57568T>C
XM_011516088.1:c.-141+57568T>C	XP_011514390.1:n.-141+57568T>C
XM_011516089.1:c.-141+57568T>C	XP_011514391.1:n.-141+57568T>C
XM_011516090.1:c.-141+57568T>C	XP_011514392.1:n.-141+57568T>C
NM_001363522.1:c.-141+57568T>C	NP_001350451.1:n.-141+57568T>C
XM_017012073.2:c.-141+57568T>C	XP_016867562.1:n.-141+57568T>C
NM_000840.3:c.-141+57568T>C MANE Select	NP_000831.2:n.-141+57568T>C
NM_001363522.2:c.-141+57568T>C	NP_001350451.1:n.-141+57568T>C