Canonical Allele Identifier: CA2261069343
Gene: SOST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755812_43755813delinsGC , CM000679.2:g.43755812_43755813delinsGC GRCh38
NC_000017.10:g.41833180_41833181delinsGC , CM000679.1:g.41833180_41833181delinsGC GRCh37
NC_000017.9:g.39188706_39188707delinsGC NCBI36
NG_008078.2:g.7976_7977delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-50_221-49delinsGC MANE Select ENSP00000301691.1:n.221-50_221-49delinsGC
ENST00000301691.2:c.221-50_221-49delinsGC ENSP00000301691.1:n.221-50_221-49delinsGC
NM_025237.2:c.221-50_221-49delinsGC NP_079513.1:n.221-50_221-49delinsGC
NM_025237.3:c.221-50_221-49delinsGC MANE Select NP_079513.1:n.221-50_221-49delinsGC