Canonical Allele Identifier: CA12481819

Gene: GRM8

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.127251397A>C , CM000669.2:g.127251397A>C	GRCh38
NC_000007.13:g.126891451A>C , CM000669.1:g.126891451A>C	GRCh37
NC_000007.12:g.126678687A>C	NCBI36
NG_029532.1:g.5978T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358373.8:c.-312+732T>G	ENSP00000351142.3:n.-312+732T>G
ENST00000706915.1:c.-312+732T>G	ENSP00000516623.1:n.-312+732T>G
ENST00000706916.1:c.-312+1400T>G	ENSP00000516624.1:n.-312+1400T>G
ENST00000706917.1:c.-416+1400T>G	ENSP00000516625.1:n.-416+1400T>G
ENST00000339582.7:c.-312+1400T>G MANE Select	ENSP00000344173.2:n.-312+1400T>G
ENST00000339582.6:c.-312+1400T>G	ENSP00000344173.2:n.-312+1400T>G
ENST00000358373.7:c.-312+732T>G	ENSP00000351142.3:n.-312+732T>G
ENST00000472701.5:c.-312+1400T>G	ENSP00000419832.1:n.-312+1400T>G
NM_001127323.1:c.-312+732T>G	NP_001120795.1:n.-312+732T>G
XM_006715938.2:c.-312+732T>G	XP_006716001.1:n.-312+732T>G
XM_011516091.1:c.-312+1400T>G	XP_011514393.1:n.-312+1400T>G
XM_011516092.1:c.-312+1400T>G	XP_011514394.1:n.-312+1400T>G
XM_011516093.1:c.-312+1400T>G	XP_011514395.1:n.-312+1400T>G
XM_006715938.4:c.-312+732T>G	XP_006716001.1:n.-312+732T>G
XM_011516091.2:c.-312+1400T>G	XP_011514393.1:n.-312+1400T>G
XM_011516092.3:c.-312+1400T>G	XP_011514394.1:n.-312+1400T>G
NM_000845.3:c.-312+1400T>G MANE Select	NP_000836.2:n.-312+1400T>G
NM_001371083.1:c.-416+1400T>G	NP_001358012.1:n.-416+1400T>G
NM_001371084.1:c.-312+732T>G	NP_001358013.1:n.-312+732T>G
NM_001371085.1:c.-312+1400T>G	NP_001358014.1:n.-312+1400T>G
NM_001371086.1:c.-312+732T>G	NP_001358015.1:n.-312+732T>G
NM_001371087.1:c.-106+1400T>G	NP_001358016.1:n.-106+1400T>G
NM_001371088.1:c.-312+732T>G	NP_001358017.1:n.-312+732T>G
NR_163849.1:n.145+1400T>G
NR_163850.1:n.145+1400T>G