Canonical Allele Identifier: CA3594594
Gene: GRM6 HGNC NCBI

Linked Data

dbSNP Id: rs757326094
ExAC: 5:178421863 C / CGCGCCAGGCCCGCCT
gnomAD v2: 5-178421863-C-CGCGCCAGGCCCGCCT
gnomAD v4: 5-178994862-C-CGCGCCAGGCCCGCCT
MyVariant Identifiers: chr5:g.178421863_178421864insGCGCCAGGCCCGCCT (hg19) chr5:g.178994862_178994863insGCGCCAGGCCCGCCT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994870_178994884dup , CM000667.2:g.178994870_178994884dup GRCh38
NC_000005.9:g.178421871_178421885dup , CM000667.1:g.178421871_178421885dup GRCh37
NC_000005.8:g.178354477_178354491dup NCBI36
NG_008105.1:g.5247_5261dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.68_82dup MANE Select ENSP00000430767.1:p.Ala27_Arg28insGlnAlaGlyLeuAla
ENST00000650031.1:c.68_82dup ENSP00000497110.1:p.Ala27_Arg28insGlnAlaGlyLeuAla
ENST00000231188.9:c.68_82dup ENSP00000231188.5:p.Ala27_Arg28insGlnAlaGlyLeuAla
ENST00000517717.1:c.68_82dup ENSP00000430767.1:p.Ala27_Arg28insGlnAlaGlyLeuAla
NM_000843.3:c.68_82dup NP_000834.2:p.Ala27_Arg28insGlnAlaGlyLeuAla
NM_000843.4:c.68_82dup MANE Select NP_000834.2:p.Ala27_Arg28insGlnAlaGlyLeuAla
Search 100 bp 5'
Search 100 bp 3'