Canonical Allele Identifier: CA4037319

Gene: GRM1

Linked Data

• ClinVar Variation Id: 447458
• ClinVar RCV Id: RCV000518761 ; RCV002525036 ; RCV003905298
• dbSNP Id: rs376313056
• ExAC: 6:146678839 C / G
• gnomAD v2: 6-146678839-C-G
• gnomAD v3: 6-146357703-C-G
• gnomAD v4: 6-146357703-C-G
• MyVariant Identifiers: chr6:g.146678839C>G (hg19) ; chr6:g.146357703C>G (hg38)
• PubMed: PMID:22558107

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.146357703C>G , CM000668.2:g.146357703C>G	GRCh38
NC_000006.11:g.146678839C>G , CM000668.1:g.146678839C>G	GRCh37
NC_000006.10:g.146720532C>G	NCBI36
NG_012839.1:g.335058C>G
NG_012839.2:g.335058C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706833.1:c.1602+9C>G	ENSP00000516579.1:n.1602+9C>G
ENST00000706834.1:c.1602+9C>G	ENSP00000516580.1:n.1602+9C>G
ENST00000706835.1:c.1602+9C>G	ENSP00000516581.1:n.1602+9C>G
ENST00000706836.1:c.1602+9C>G	ENSP00000516582.1:n.1602+9C>G
ENST00000282753.6:c.1602+9C>G MANE Select	ENSP00000282753.1:n.1602+9C>G
ENST00000282753.5:c.1602+9C>G	ENSP00000282753.1:n.1602+9C>G
ENST00000355289.8:c.1602+9C>G	ENSP00000347437.4:n.1602+9C>G
ENST00000361719.6:c.1602+9C>G	ENSP00000354896.2:n.1602+9C>G
ENST00000492807.6:c.1602+9C>G	ENSP00000424095.1:n.1602+9C>G
ENST00000507907.1:c.1602+9C>G	ENSP00000425599.1:n.1602+9C>G
NM_001278064.1:c.1602+9C>G	NP_001264993.1:n.1602+9C>G
NM_001278065.1:c.1602+9C>G	NP_001264994.1:n.1602+9C>G
NM_001278066.1:c.1602+9C>G	NP_001264995.1:n.1602+9C>G
NM_001278067.1:c.1602+9C>G	NP_001264996.1:n.1602+9C>G
XM_011535782.1:c.1602+9C>G	XP_011534084.1:n.1602+9C>G
XM_011535783.1:c.1602+9C>G	XP_011534085.1:n.1602+9C>G
XM_011535784.1:c.1602+9C>G	XP_011534086.1:n.1602+9C>G
XM_017010783.1:c.1602+9C>G	XP_016866272.1:n.1602+9C>G
XM_017010784.1:c.1602+9C>G	XP_016866273.1:n.1602+9C>G
XM_017010785.1:c.1602+9C>G	XP_016866274.1:n.1602+9C>G
XM_017010786.1:c.1602+9C>G	XP_016866275.1:n.1602+9C>G
XM_017010787.1:c.1602+9C>G	XP_016866276.1:n.1602+9C>G
XM_017010788.1:c.375+9C>G	XP_016866277.1:n.375+9C>G
XM_024446412.1:c.1602+9C>G	XP_024302180.1:n.1602+9C>G
NM_001278064.2:c.1602+9C>G MANE Select	NP_001264993.1:n.1602+9C>G
NM_001278065.2:c.1602+9C>G	NP_001264994.1:n.1602+9C>G