Canonical Allele Identifier: CA2676848195
Gene: GRM6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994643_178994657dup , CM000667.2:g.178994643_178994657dup GRCh38
NC_000005.9:g.178421644_178421658dup , CM000667.1:g.178421644_178421658dup GRCh37
NC_000005.8:g.178354250_178354264dup NCBI36
NG_008105.1:g.5475_5489dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.296_310dup MANE Select ENSP00000430767.1:p.Thr103_Tyr104insCysSerArgAspThr
ENST00000650031.1:c.296_310dup ENSP00000497110.1:p.Thr103_Tyr104insCysSerArgAspThr
ENST00000231188.9:c.296_310dup ENSP00000231188.5:p.Thr103_Tyr104insCysSerArgAspThr
ENST00000517717.1:c.296_310dup ENSP00000430767.1:p.Thr103_Tyr104insCysSerArgAspThr
NM_000843.3:c.296_310dup NP_000834.2:p.Thr103_Tyr104insCysSerArgAspThr
NM_000843.4:c.296_310dup MANE Select NP_000834.2:p.Thr103_Tyr104insCysSerArgAspThr