Canonical Allele Identifier: CA917651925
Gene: GRM6 HGNC NCBI

Linked Data

dbSNP Id: rs1554113934

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178988982del , CM000667.2:g.178988982del GRCh38
NC_000005.9:g.178415983del , CM000667.1:g.178415983del GRCh37
NC_000005.8:g.178348589del NCBI36
NG_008105.1:g.11142del

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.1307del MANE Select ENSP00000430767.1:p.Thr436MetfsTer23
ENST00000650031.1:c.1307del ENSP00000497110.1:p.Thr436MetfsTer23
ENST00000231188.9:c.1307del ENSP00000231188.5:p.Thr436MetfsTer23
ENST00000517717.1:c.1307del ENSP00000430767.1:p.Thr436MetfsTer23
NM_000843.3:c.1307del NP_000834.2:p.Thr436MetfsTer23
XR_941310.1:n.1470-765del
NM_000843.4:c.1307del MANE Select NP_000834.2:p.Thr436MetfsTer23