Canonical Allele Identifier: CA564902053

Gene: GRM6

Linked Data

• dbSNP Id: rs1420043222
• gnomAD v2: 5-178421664-CCG-C
• gnomAD v4: 5-178994663-CCG-C
• MyVariant Identifiers: chr5:g.178421665_178421666del (hg19) ; chr5:g.178994664_178994665del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.178994669_178994670del , CM000667.2:g.178994669_178994670del	GRCh38
NC_000005.9:g.178421670_178421671del , CM000667.1:g.178421670_178421671del	GRCh37
NC_000005.8:g.178354276_178354277del	NCBI36
NG_008105.1:g.5459_5460del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517717.3:c.280_281del MANE Select	ENSP00000430767.1:p.Arg94AlafsTer?
ENST00000650031.1:c.280_281del	ENSP00000497110.1:p.Arg94AlafsTer?
ENST00000231188.9:c.280_281del	ENSP00000231188.5:p.Arg94AlafsTer?
ENST00000517717.1:c.280_281del	ENSP00000430767.1:p.Arg94AlafsTer?
NM_000843.3:c.280_281del	NP_000834.2:p.Arg94AlafsTer?
NM_000843.4:c.280_281del MANE Select	NP_000834.2:p.Arg94AlafsTer?