Canonical Allele Identifier: CA136960352
Gene: GRM4 HGNC NCBI

Linked Data

dbSNP Id: rs733457
gnomAD v2: 6-34068408-G-A
gnomAD v3: 6-34100631-G-A
gnomAD v4: 6-34100631-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34100631G>A , CM000668.2:g.34100631G>A GRCh38
NC_000006.11:g.34068408G>A , CM000668.1:g.34068408G>A GRCh37
NC_000006.10:g.34176386G>A NCBI36
NG_029677.3:g.59992C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000538487.7:c.520-8532C>T MANE Select ENSP00000440556.1:n.520-8532C>T
ENST00000374177.7:c.313-8532C>T ENSP00000363292.3:n.313-8532C>T
ENST00000374181.8:c.520-8532C>T ENSP00000363296.4:n.520-8532C>T
ENST00000455714.6:c.99+1391C>T ENSP00000398456.2:n.99+1391C>T
ENST00000535756.5:c.120+2950C>T ENSP00000437925.1:n.120+2950C>T
ENST00000538487.6:c.520-8532C>T ENSP00000440556.1:n.520-8532C>T
ENST00000544773.6:c.13-8532C>T ENSP00000437730.1:n.13-8532C>T
ENST00000607916.1:n.489-8532C>T
ENST00000609222.5:c.120+2950C>T ENSP00000477466.1:n.120+2950C>T
ENST00000609278.1:c.519+32347C>T ENSP00000477016.1:n.519+32347C>T
ENST00000609973.1:n.45-8532C>T
NM_000841.3:c.520-8532C>T NP_000832.1:n.520-8532C>T
NM_001256809.2:c.313-8532C>T NP_001243738.1:n.313-8532C>T
NM_001256811.2:c.520-8532C>T NP_001243740.1:n.520-8532C>T
NM_001256812.2:c.13-8532C>T NP_001243741.1:n.13-8532C>T
NM_001256813.2:c.120+2950C>T NP_001243742.1:n.120+2950C>T
NM_001282847.1:c.-189+32347C>T NP_001269776.1:n.-189+32347C>T
XM_017010790.2:c.520-8532C>T XP_016866279.1:n.520-8532C>T
XM_017010791.2:c.520-8532C>T XP_016866280.1:n.520-8532C>T
XM_017010792.1:c.279+1391C>T XP_016866281.1:n.279+1391C>T
XM_017010793.2:c.120+2950C>T XP_016866282.1:n.120+2950C>T
XR_001743363.1:n.1014-8532C>T
XR_001743364.2:n.629+2950C>T
NM_000841.4:c.520-8532C>T MANE Select NP_000832.1:n.520-8532C>T
NM_001256813.3:c.120+2950C>T NP_001243742.1:n.120+2950C>T
NM_001282847.2:c.-189+32347C>T NP_001269776.1:n.-189+32347C>T
NM_001256809.3:c.313-8532C>T NP_001243738.1:n.313-8532C>T
NM_001256811.3:c.520-8532C>T NP_001243740.1:n.520-8532C>T