Canonical Allele Identifier: CA1723318224
Gene: GRM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815547_86815551delinsATTAT , CM000669.2:g.86815547_86815551delinsATTAT GRCh38
NC_000007.13:g.86444863_86444867delinsATTAT , CM000669.1:g.86444863_86444867delinsATTAT GRCh37
NC_000007.12:g.86282799_86282803delinsATTAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-23292_1325-23288delinsATTAT MANE Select ENSP00000355316.2:n.1325-23292_1325-23288delinsATTAT
ENST00000361669.6:c.1325-23292_1325-23288delinsATTAT ENSP00000355316.2:n.1325-23292_1325-23288delinsATTAT
ENST00000439827.1:c.1324+28431_1324+28435delinsATTAT ENSP00000398767.1:n.1324+28431_1324+28435delinsATTAT
NM_000840.2:c.1325-23292_1325-23288delinsATTAT NP_000831.2:n.1325-23292_1325-23288delinsATTAT
XM_011516088.1:c.1324+28431_1324+28435delinsATTAT XP_011514390.1:n.1324+28431_1324+28435delinsATTAT
XM_011516090.1:c.1325-17475_1325-17471delinsATTAT XP_011514392.1:n.1325-17475_1325-17471delinsATTAT
NM_001363522.1:c.1324+28431_1324+28435delinsATTAT NP_001350451.1:n.1324+28431_1324+28435delinsATTAT
NM_000840.3:c.1325-23292_1325-23288delinsATTAT MANE Select NP_000831.2:n.1325-23292_1325-23288delinsATTAT
NM_001363522.2:c.1324+28431_1324+28435delinsATTAT NP_001350451.1:n.1324+28431_1324+28435delinsATTAT