Canonical Allele Identifier: CA1723318202
Gene: GRM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815487_86815488delinsCA , CM000669.2:g.86815487_86815488delinsCA GRCh38
NC_000007.13:g.86444803_86444804delinsCA , CM000669.1:g.86444803_86444804delinsCA GRCh37
NC_000007.12:g.86282739_86282740delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-23352_1325-23351delinsCA MANE Select ENSP00000355316.2:n.1325-23352_1325-23351delinsCA
ENST00000361669.6:c.1325-23352_1325-23351delinsCA ENSP00000355316.2:n.1325-23352_1325-23351delinsCA
ENST00000439827.1:c.1324+28371_1324+28372delinsCA ENSP00000398767.1:n.1324+28371_1324+28372delinsCA
NM_000840.2:c.1325-23352_1325-23351delinsCA NP_000831.2:n.1325-23352_1325-23351delinsCA
XM_011516088.1:c.1324+28371_1324+28372delinsCA XP_011514390.1:n.1324+28371_1324+28372delinsCA
XM_011516090.1:c.1325-17535_1325-17534delinsCA XP_011514392.1:n.1325-17535_1325-17534delinsCA
NM_001363522.1:c.1324+28371_1324+28372delinsCA NP_001350451.1:n.1324+28371_1324+28372delinsCA
NM_000840.3:c.1325-23352_1325-23351delinsCA MANE Select NP_000831.2:n.1325-23352_1325-23351delinsCA
NM_001363522.2:c.1324+28371_1324+28372delinsCA NP_001350451.1:n.1324+28371_1324+28372delinsCA