Canonical Allele Identifier: CA12520473
Gene: GRM8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.126684537A>G , CM000669.2:g.126684537A>G GRCh38
NC_000007.13:g.126324591A>G , CM000669.1:g.126324591A>G GRCh37
NC_000007.12:g.126111827A>G NCBI36
NG_029532.1:g.572838T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358373.8:c.1358-75039T>C ENSP00000351142.3:n.1358-75039T>C
ENST00000706915.1:c.1358-75039T>C ENSP00000516623.1:n.1358-75039T>C
ENST00000706916.1:c.1358-75039T>C ENSP00000516624.1:n.1358-75039T>C
ENST00000706917.1:c.1358-75039T>C ENSP00000516625.1:n.1358-75039T>C
ENST00000339582.7:c.1358-75039T>C MANE Select ENSP00000344173.2:n.1358-75039T>C
ENST00000339582.6:c.1358-75039T>C ENSP00000344173.2:n.1358-75039T>C
ENST00000341617.7:c.1428+17220T>C ENSP00000345747.3:n.1428+17220T>C
ENST00000358373.7:c.1358-75039T>C ENSP00000351142.3:n.1358-75039T>C
ENST00000472701.5:c.1358-75039T>C ENSP00000419832.1:n.1358-75039T>C
ENST00000480995.5:n.1145+17220T>C
NM_000845.2:c.1358-75039T>C NP_000836.2:n.1358-75039T>C
NM_001127323.1:c.1358-75039T>C NP_001120795.1:n.1358-75039T>C
NR_028041.1:n.1739+17220T>C
XM_006715938.2:c.1358-75039T>C XP_006716001.1:n.1358-75039T>C
XM_011516091.1:c.1358-75039T>C XP_011514393.1:n.1358-75039T>C
XM_011516092.1:c.1358-75039T>C XP_011514394.1:n.1358-75039T>C
XM_011516093.1:c.1358-75039T>C XP_011514395.1:n.1358-75039T>C
XM_011516094.1:c.875-75039T>C XP_011514396.1:n.875-75039T>C
XM_011516095.1:c.776-75039T>C XP_011514397.1:n.776-75039T>C
XM_011516096.1:c.743-75039T>C XP_011514398.1:n.743-75039T>C
XM_011516097.1:c.743-75039T>C XP_011514399.1:n.743-75039T>C
XM_011516098.1:c.743-75039T>C XP_011514400.1:n.743-75039T>C
XM_011516099.1:c.743-75039T>C XP_011514401.1:n.743-75039T>C
XM_011516100.1:c.743-75039T>C XP_011514402.1:n.743-75039T>C
XM_011516101.1:c.743-75039T>C XP_011514403.1:n.743-75039T>C
XM_011516102.1:c.743-75039T>C XP_011514404.1:n.743-75039T>C
XM_011516103.1:c.521-75039T>C XP_011514405.1:n.521-75039T>C
XM_011516104.1:c.521-75039T>C XP_011514406.1:n.521-75039T>C
XM_011516105.1:c.521-75039T>C XP_011514407.1:n.521-75039T>C
XM_011516106.1:c.521-75039T>C XP_011514408.1:n.521-75039T>C
XM_011516107.1:c.521-75039T>C XP_011514409.1:n.521-75039T>C
XM_011516108.1:c.290-75039T>C XP_011514410.1:n.290-75039T>C
XM_011516109.1:c.125-75039T>C XP_011514411.1:n.125-75039T>C
XM_006715938.4:c.1358-75039T>C XP_006716001.1:n.1358-75039T>C
XM_011516091.2:c.1358-75039T>C XP_011514393.1:n.1358-75039T>C
XM_011516092.3:c.1358-75039T>C XP_011514394.1:n.1358-75039T>C
XM_011516095.2:c.776-75039T>C XP_011514397.1:n.776-75039T>C
XM_011516101.2:c.743-75039T>C XP_011514403.1:n.743-75039T>C
XM_011516102.2:c.743-75039T>C XP_011514404.1:n.743-75039T>C
XM_011516103.2:c.521-75039T>C XP_011514405.1:n.521-75039T>C
XM_011516108.2:c.290-75039T>C XP_011514410.1:n.290-75039T>C
XM_017012074.1:c.1358-75039T>C XP_016867563.1:n.1358-75039T>C
XM_017012075.1:c.743-75039T>C XP_016867564.1:n.743-75039T>C
XM_017012076.1:c.743-75039T>C XP_016867565.1:n.743-75039T>C
XM_017012077.1:c.743-75039T>C XP_016867566.1:n.743-75039T>C
XM_017012078.1:c.743-75039T>C XP_016867567.1:n.743-75039T>C
XM_017012079.1:c.743-75039T>C XP_016867568.1:n.743-75039T>C
XM_017012080.1:c.521-75039T>C XP_016867569.1:n.521-75039T>C
XM_024446736.1:c.521-75039T>C XP_024302504.1:n.521-75039T>C
NM_000845.3:c.1358-75039T>C MANE Select NP_000836.2:n.1358-75039T>C
NM_001371083.1:c.1358-75039T>C NP_001358012.1:n.1358-75039T>C
NM_001371084.1:c.1358-75039T>C NP_001358013.1:n.1358-75039T>C
NM_001371085.1:c.1358-75039T>C NP_001358014.1:n.1358-75039T>C
NM_001371086.1:c.1358-75039T>C NP_001358015.1:n.1358-75039T>C
NM_001371087.1:c.743-75039T>C NP_001358016.1:n.743-75039T>C
NR_163849.1:n.1814-75039T>C
NR_163850.1:n.993-75039T>C
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