Canonical Allele Identifier: CA808240290
Gene: GRM6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2141400
ClinVar RCV Id: RCV003056940
dbSNP Id: rs1419288852
gnomAD v3: 5-178994580-T-TCGCCGC
gnomAD v4: 5-178994580-T-TCGCCGC
MyVariant Identifiers: chr5:g.178421581_178421582insCGCCGC (hg19) chr5:g.178994580_178994581insCGCCGC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994581_178994586dup , CM000667.2:g.178994581_178994586dup GRCh38
NC_000005.9:g.178421582_178421587dup , CM000667.1:g.178421582_178421587dup GRCh37
NC_000005.8:g.178354188_178354193dup NCBI36
NG_008105.1:g.5538_5543dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.359_364dup MANE Select ENSP00000430767.1:p.Gly121_Asp122insGlyGly
ENST00000650031.1:c.359_364dup ENSP00000497110.1:p.Gly121_Asp122insGlyGly
ENST00000231188.9:c.359_364dup ENSP00000231188.5:p.Gly121_Asp122insGlyGly
ENST00000517717.1:c.359_364dup ENSP00000430767.1:p.Gly121_Asp122insGlyGly
NM_000843.3:c.359_364dup NP_000834.2:p.Gly121_Asp122insGlyGly
NM_000843.4:c.359_364dup MANE Select NP_000834.2:p.Gly121_Asp122insGlyGly
Search 100 bp 5'
Search 100 bp 3'