Canonical Allele Identifier: CA1723318194
Gene: GRM3 HGNC NCBI

Linked Data

dbSNP Id: rs1797997361

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815478dup , CM000669.2:g.86815478dup GRCh38
NC_000007.13:g.86444794dup , CM000669.1:g.86444794dup GRCh37
NC_000007.12:g.86282730dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-23361dup MANE Select ENSP00000355316.2:n.1325-23361dup
ENST00000361669.6:c.1325-23361dup ENSP00000355316.2:n.1325-23361dup
ENST00000439827.1:c.1324+28362dup ENSP00000398767.1:n.1324+28362dup
NM_000840.2:c.1325-23361dup NP_000831.2:n.1325-23361dup
XM_011516088.1:c.1324+28362dup XP_011514390.1:n.1324+28362dup
XM_011516090.1:c.1325-17544dup XP_011514392.1:n.1325-17544dup
NM_001363522.1:c.1324+28362dup NP_001350451.1:n.1324+28362dup
NM_000840.3:c.1325-23361dup MANE Select NP_000831.2:n.1325-23361dup
NM_001363522.2:c.1324+28362dup NP_001350451.1:n.1324+28362dup