Canonical Allele Identifier: CA1723318205
Gene: GRM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815493_86815497delinsAAAGT , CM000669.2:g.86815493_86815497delinsAAAGT GRCh38
NC_000007.13:g.86444809_86444813delinsAAAGT , CM000669.1:g.86444809_86444813delinsAAAGT GRCh37
NC_000007.12:g.86282745_86282749delinsAAAGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-23346_1325-23342delinsAAAGT MANE Select ENSP00000355316.2:n.1325-23346_1325-23342delinsAAAGT
ENST00000361669.6:c.1325-23346_1325-23342delinsAAAGT ENSP00000355316.2:n.1325-23346_1325-23342delinsAAAGT
ENST00000439827.1:c.1324+28377_1324+28381delinsAAAGT ENSP00000398767.1:n.1324+28377_1324+28381delinsAAAGT
NM_000840.2:c.1325-23346_1325-23342delinsAAAGT NP_000831.2:n.1325-23346_1325-23342delinsAAAGT
XM_011516088.1:c.1324+28377_1324+28381delinsAAAGT XP_011514390.1:n.1324+28377_1324+28381delinsAAAGT
XM_011516090.1:c.1325-17529_1325-17525delinsAAAGT XP_011514392.1:n.1325-17529_1325-17525delinsAAAGT
NM_001363522.1:c.1324+28377_1324+28381delinsAAAGT NP_001350451.1:n.1324+28377_1324+28381delinsAAAGT
NM_000840.3:c.1325-23346_1325-23342delinsAAAGT MANE Select NP_000831.2:n.1325-23346_1325-23342delinsAAAGT
NM_001363522.2:c.1324+28377_1324+28381delinsAAAGT NP_001350451.1:n.1324+28377_1324+28381delinsAAAGT