Canonical Allele Identifier: CA2261069316
Gene: SOST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755785_43755801delinsAGGGTGGCCGCCCGCCT , CM000679.2:g.43755785_43755801delinsAGGGTGGCCGCCCGCCT GRCh38
NC_000017.10:g.41833153_41833169delinsAGGGTGGCCGCCCGCCT , CM000679.1:g.41833153_41833169delinsAGGGTGGCCGCCCGCCT GRCh37
NC_000017.9:g.39188679_39188695delinsAGGGTGGCCGCCCGCCT NCBI36
NG_008078.2:g.7988_8004delinsAGGCGGGCGGCCACCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-38_221-22delinsAGGCGGGCGGCCACCCT MANE Select ENSP00000301691.1:n.221-38_221-22delinsAGGCGGGCGGCCACCCT
ENST00000301691.2:c.221-38_221-22delinsAGGCGGGCGGCCACCCT ENSP00000301691.1:n.221-38_221-22delinsAGGCGGGCGGCCACCCT
NM_025237.2:c.221-38_221-22delinsAGGCGGGCGGCCACCCT NP_079513.1:n.221-38_221-22delinsAGGCGGGCGGCCACCCT
NM_025237.3:c.221-38_221-22delinsAGGCGGGCGGCCACCCT MANE Select NP_079513.1:n.221-38_221-22delinsAGGCGGGCGGCCACCCT