Canonical Allele Identifier: CA2261069086
Gene: SOST HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755325_43755326delinsAG , CM000679.2:g.43755325_43755326delinsAG GRCh38
NC_000017.10:g.41832693_41832694delinsAG , CM000679.1:g.41832693_41832694delinsAG GRCh37
NC_000017.9:g.39188219_39188220delinsAG NCBI36
NG_008078.2:g.8463_8464delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.*16_*17delinsCT MANE Select ENSP00000301691.1:n.*16_*17delinsCT
ENST00000301691.2:c.*16_*17delinsCT ENSP00000301691.1:n.*16_*17delinsCT
NM_025237.2:c.*16_*17delinsCT NP_079513.1:n.*16_*17delinsCT
NM_025237.3:c.*16_*17delinsCT MANE Select NP_079513.1:n.*16_*17delinsCT
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