Canonical Allele Identifier: CA2261069073
Gene: SOST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755307_43755332delinsGGGCGCCCGCCGGTGGGGAGGGGCGC , CM000679.2:g.43755307_43755332delinsGGGCGCCCGCCGGTGGGGAGGGGCGC GRCh38
NC_000017.10:g.41832675_41832700delinsGGGCGCCCGCCGGTGGGGAGGGGCGC , CM000679.1:g.41832675_41832700delinsGGGCGCCCGCCGGTGGGGAGGGGCGC GRCh37
NC_000017.9:g.39188201_39188226delinsGGGCGCCCGCCGGTGGGGAGGGGCGC NCBI36
NG_008078.2:g.8457_8482delinsGCGCCCCTCCCCACCGGCGGGCGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.*10_*35delinsGCGCCCCTCCCCACCGGCGGGCGCCC MANE Select ENSP00000301691.1:n.*10_*35delinsGCGCCCCTCCCCACCGGCGGGCGCCC
ENST00000301691.2:c.*10_*35delinsGCGCCCCTCCCCACCGGCGGGCGCCC ENSP00000301691.1:n.*10_*35delinsGCGCCCCTCCCCACCGGCGGGCGCCC
NM_025237.2:c.*10_*35delinsGCGCCCCTCCCCACCGGCGGGCGCCC NP_079513.1:n.*10_*35delinsGCGCCCCTCCCCACCGGCGGGCGCCC
NM_025237.3:c.*10_*35delinsGCGCCCCTCCCCACCGGCGGGCGCCC MANE Select NP_079513.1:n.*10_*35delinsGCGCCCCTCCCCACCGGCGGGCGCCC