Canonical Allele Identifier: CA843335622
Gene: GRM3 HGNC NCBI

Linked Data

dbSNP Id: rs1321077707

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815518del , CM000669.2:g.86815518del GRCh38
NC_000007.13:g.86444834del , CM000669.1:g.86444834del GRCh37
NC_000007.12:g.86282770del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-23321del MANE Select ENSP00000355316.2:n.1325-23321del
ENST00000361669.6:c.1325-23321del ENSP00000355316.2:n.1325-23321del
ENST00000439827.1:c.1324+28402del ENSP00000398767.1:n.1324+28402del
NM_000840.2:c.1325-23321del NP_000831.2:n.1325-23321del
XM_011516088.1:c.1324+28402del XP_011514390.1:n.1324+28402del
XM_011516090.1:c.1325-17504del XP_011514392.1:n.1325-17504del
NM_001363522.1:c.1324+28402del NP_001350451.1:n.1324+28402del
NM_000840.3:c.1325-23321del MANE Select NP_000831.2:n.1325-23321del
NM_001363522.2:c.1324+28402del NP_001350451.1:n.1324+28402del