Canonical Allele Identifier: CA1723318238
Gene: GRM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815581_86815584delinsTCTC , CM000669.2:g.86815581_86815584delinsTCTC GRCh38
NC_000007.13:g.86444897_86444900delinsTCTC , CM000669.1:g.86444897_86444900delinsTCTC GRCh37
NC_000007.12:g.86282833_86282836delinsTCTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-23258_1325-23255delinsTCTC MANE Select ENSP00000355316.2:n.1325-23258_1325-23255delinsTCTC
ENST00000361669.6:c.1325-23258_1325-23255delinsTCTC ENSP00000355316.2:n.1325-23258_1325-23255delinsTCTC
ENST00000439827.1:c.1324+28465_1324+28468delinsTCTC ENSP00000398767.1:n.1324+28465_1324+28468delinsTCTC
NM_000840.2:c.1325-23258_1325-23255delinsTCTC NP_000831.2:n.1325-23258_1325-23255delinsTCTC
XM_011516088.1:c.1324+28465_1324+28468delinsTCTC XP_011514390.1:n.1324+28465_1324+28468delinsTCTC
XM_011516090.1:c.1325-17441_1325-17438delinsTCTC XP_011514392.1:n.1325-17441_1325-17438delinsTCTC
NM_001363522.1:c.1324+28465_1324+28468delinsTCTC NP_001350451.1:n.1324+28465_1324+28468delinsTCTC
NM_000840.3:c.1325-23258_1325-23255delinsTCTC MANE Select NP_000831.2:n.1325-23258_1325-23255delinsTCTC
NM_001363522.2:c.1324+28465_1324+28468delinsTCTC NP_001350451.1:n.1324+28465_1324+28468delinsTCTC