Canonical Allele Identifier: CA1723298087
Gene: GRM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86792916T= , CM000669.2:g.86792916T= GRCh38
NC_000007.13:g.86422232T= , CM000669.1:g.86422232T= GRCh37
NC_000007.12:g.86260168T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_000840.3:c.1324+5800T= MANE Select NP_000831.2:n.1324+5800T=
ENST00000361669.7:c.1324+5800T= MANE Select ENSP00000355316.2:n.1324+5800T=
NM_000840.2:c.1324+5800T= NP_000831.2:n.1324+5800T=
NM_001363522.1:c.1324+5800T= NP_001350451.1:n.1324+5800T=
NM_001363522.2:c.1324+5800T= NP_001350451.1:n.1324+5800T=
ENST00000361669.6:c.1324+5800T= ENSP00000355316.2:n.1324+5800T=
ENST00000439827.1:c.1324+5800T= ENSP00000398767.1:n.1324+5800T=
XM_011516088.1:c.1324+5800T= XP_011514390.1:n.1324+5800T=
XM_011516089.1:c.1324+5800T= XP_011514391.1:n.1324+5800T=
XM_011516090.1:c.1324+5800T= XP_011514392.1:n.1324+5800T=
XM_017012073.2:c.1325-132T= XP_016867562.1:n.1325-132T=
XR_002956570.1:n.90+271A=
XR_002956571.1:n.88+1704A=
XR_927721.1:n.1425+271A=