Canonical Allele Identifier: CA808240613
Gene: GRM6 HGNC NCBI

Linked Data

dbSNP Id: rs1403095260

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994861_178994875dup , CM000667.2:g.178994861_178994875dup GRCh38
NC_000005.9:g.178421862_178421876dup , CM000667.1:g.178421862_178421876dup GRCh37
NC_000005.8:g.178354468_178354482dup NCBI36
NG_008105.1:g.5253_5267dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.74_88dup MANE Select ENSP00000430767.1:p.Ala29_Ala30insGlyLeuAlaArgAla
ENST00000650031.1:c.74_88dup ENSP00000497110.1:p.Ala29_Ala30insGlyLeuAlaArgAla
ENST00000231188.9:c.74_88dup ENSP00000231188.5:p.Ala29_Ala30insGlyLeuAlaArgAla
ENST00000517717.1:c.74_88dup ENSP00000430767.1:p.Ala29_Ala30insGlyLeuAlaArgAla
NM_000843.3:c.74_88dup NP_000834.2:p.Ala29_Ala30insGlyLeuAlaArgAla
NM_000843.4:c.74_88dup MANE Select NP_000834.2:p.Ala29_Ala30insGlyLeuAlaArgAla