Canonical Allele Identifier: CA2676848231

Gene: GRM6

Linked Data

• gnomAD v4: 5-178994768-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.178994769del , CM000667.2:g.178994769del	GRCh38
NC_000005.9:g.178421770del , CM000667.1:g.178421770del	GRCh37
NC_000005.8:g.178354376del	NCBI36
NG_008105.1:g.5355del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517717.3:c.176del MANE Select	ENSP00000430767.1:p.Gln59ArgfsTer2
ENST00000650031.1:c.176del	ENSP00000497110.1:p.Gln59ArgfsTer2
ENST00000231188.9:c.176del	ENSP00000231188.5:p.Gln59ArgfsTer2
ENST00000517717.1:c.176del	ENSP00000430767.1:p.Gln59ArgfsTer2
NM_000843.3:c.176del	NP_000834.2:p.Gln59ArgfsTer2
NM_000843.4:c.176del MANE Select	NP_000834.2:p.Gln59ArgfsTer2