Canonical Allele Identifier: CA2261069331

Gene: SOST

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43755800_43755801delinsCT , CM000679.2:g.43755800_43755801delinsCT	GRCh38
NC_000017.10:g.41833168_41833169delinsCT , CM000679.1:g.41833168_41833169delinsCT	GRCh37
NC_000017.9:g.39188694_39188695delinsCT	NCBI36
NG_008078.2:g.7988_7989delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301691.3:c.221-38_221-37delinsAG MANE Select	ENSP00000301691.1:n.221-38_221-37delinsAG
ENST00000301691.2:c.221-38_221-37delinsAG	ENSP00000301691.1:n.221-38_221-37delinsAG
NM_025237.2:c.221-38_221-37delinsAG	NP_079513.1:n.221-38_221-37delinsAG
NM_025237.3:c.221-38_221-37delinsAG MANE Select	NP_079513.1:n.221-38_221-37delinsAG