Canonical Allele Identifier: CA2580074086
Gene: GRM6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1949549
ClinVar RCV Id: RCV002676301
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178988980_178988981delinsTG , CM000667.2:g.178988980_178988981delinsTG GRCh38
NC_000005.9:g.178415981_178415982delinsTG , CM000667.1:g.178415981_178415982delinsTG GRCh37
NC_000005.8:g.178348587_178348588delinsTG NCBI36
NG_008105.1:g.11143_11144delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000517717.3:c.1308_1309delinsCA MANE Select ENSP00000430767.1:p.Asp437Asn
ENST00000650031.1:c.1308_1309delinsCA ENSP00000497110.1:p.Asp437Asn
ENST00000231188.9:c.1308_1309delinsCA ENSP00000231188.5:p.Asp437Asn
ENST00000517717.1:c.1308_1309delinsCA ENSP00000430767.1:p.Asp437Asn
NM_000843.3:c.1308_1309delinsCA NP_000834.2:p.Asp437Asn
XR_941310.1:n.1470-767_1470-766delinsTG
NM_000843.4:c.1308_1309delinsCA MANE Select NP_000834.2:p.Asp437Asn
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Search 100 bp 3'