Canonical Allele Identifier: CA808240604
Gene: GRM6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2049899
ClinVar RCV Id: RCV002937330
dbSNP Id: rs1308648283
gnomAD v3: 5-178994851-AGCCCGCCGCGCGCGCCAG-A
gnomAD v4: 5-178994851-AGCCCGCCGCGCGCGCCAG-A
MyVariant Identifiers: chr5:g.178421853_178421870del (hg19) chr5:g.178994852_178994869del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994859_178994876del , CM000667.2:g.178994859_178994876del GRCh38
NC_000005.9:g.178421860_178421877del , CM000667.1:g.178421860_178421877del GRCh37
NC_000005.8:g.178354466_178354483del NCBI36
NG_008105.1:g.5255_5272del

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.76_93del MANE Select ENSP00000430767.1:p.Leu26_Gly31del
ENST00000650031.1:c.76_93del ENSP00000497110.1:p.Leu26_Gly31del
ENST00000231188.9:c.76_93del ENSP00000231188.5:p.Leu26_Gly31del
ENST00000517717.1:c.76_93del ENSP00000430767.1:p.Leu26_Gly31del
NM_000843.3:c.76_93del NP_000834.2:p.Leu26_Gly31del
NM_000843.4:c.76_93del MANE Select NP_000834.2:p.Leu26_Gly31del
Search 100 bp 5'
Search 100 bp 3'