Canonical Allele Identifier: CA2497130606
Gene: GRM6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1938719
ClinVar RCV Id: RCV002662778
dbSNP Id: rs1760739257
gnomAD v4: 5-178994607-A-ACGAAGCTCAGCGCCTGCT
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994609_178994626dup , CM000667.2:g.178994609_178994626dup GRCh38
NC_000005.9:g.178421610_178421627dup , CM000667.1:g.178421610_178421627dup GRCh37
NC_000005.8:g.178354216_178354233dup NCBI36
NG_008105.1:g.5499_5516dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.320_337dup MANE Select ENSP00000430767.1:p.Phe112_Val113insGluGlnAlaLeuSerPhe
ENST00000650031.1:c.320_337dup ENSP00000497110.1:p.Phe112_Val113insGluGlnAlaLeuSerPhe
ENST00000231188.9:c.320_337dup ENSP00000231188.5:p.Phe112_Val113insGluGlnAlaLeuSerPhe
ENST00000517717.1:c.320_337dup ENSP00000430767.1:p.Phe112_Val113insGluGlnAlaLeuSerPhe
NM_000843.3:c.320_337dup NP_000834.2:p.Phe112_Val113insGluGlnAlaLeuSerPhe
NM_000843.4:c.320_337dup MANE Select NP_000834.2:p.Phe112_Val113insGluGlnAlaLeuSerPhe
Search 100 bp 5'
Search 100 bp 3'