Canonical Allele Identifier: CA564902078
Gene: GRM6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1146066
ClinVar RCV Id: RCV001485184
dbSNP Id: rs1189206125
gnomAD v2: 5-178421873-CCGCCTGCGCCAGCCA-C
gnomAD v3: 5-178994872-CCGCCTGCGCCAGCCA-C
gnomAD v4: 5-178994872-CCGCCTGCGCCAGCCA-C
MyVariant Identifiers: chr5:g.178421874_178421888del (hg19) chr5:g.178994873_178994887del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994877_178994891del , CM000667.2:g.178994877_178994891del GRCh38
NC_000005.9:g.178421878_178421892del , CM000667.1:g.178421878_178421892del GRCh37
NC_000005.8:g.178354484_178354498del NCBI36
NG_008105.1:g.5237_5251del

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.58_72del MANE Select ENSP00000430767.1:p.Trp20_Ala24del
ENST00000650031.1:c.58_72del ENSP00000497110.1:p.Trp20_Ala24del
ENST00000231188.9:c.58_72del ENSP00000231188.5:p.Trp20_Ala24del
ENST00000517717.1:c.58_72del ENSP00000430767.1:p.Trp20_Ala24del
NM_000843.3:c.58_72del NP_000834.2:p.Trp20_Ala24del
NM_000843.4:c.58_72del MANE Select NP_000834.2:p.Trp20_Ala24del
Search 100 bp 5'
Search 100 bp 3'