Canonical Allele Identifier: CA2676848211

Gene: GRM6

Linked Data

• gnomAD v4: 5-178994683-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.178994683_178994684insT , CM000667.2:g.178994683_178994684insT	GRCh38
NC_000005.9:g.178421684_178421685insT , CM000667.1:g.178421684_178421685insT	GRCh37
NC_000005.8:g.178354290_178354291insT	NCBI36
NG_008105.1:g.5440_5441insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517717.3:c.261_262insA MANE Select	ENSP00000430767.1:p.Gly88ArgfsTer?
ENST00000650031.1:c.261_262insA	ENSP00000497110.1:p.Gly88ArgfsTer?
ENST00000231188.9:c.261_262insA	ENSP00000231188.5:p.Gly88ArgfsTer?
ENST00000517717.1:c.261_262insA	ENSP00000430767.1:p.Gly88ArgfsTer?
NM_000843.3:c.261_262insA	NP_000834.2:p.Gly88ArgfsTer?
NM_000843.4:c.261_262insA MANE Select	NP_000834.2:p.Gly88ArgfsTer?