Canonical Allele Identifier: CA2261069098

Gene: SOST

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43755342_43755345delinsCTAG , CM000679.2:g.43755342_43755345delinsCTAG	GRCh38
NC_000017.10:g.41832710_41832713delinsCTAG , CM000679.1:g.41832710_41832713delinsCTAG	GRCh37
NC_000017.9:g.39188236_39188239delinsCTAG	NCBI36
NG_008078.2:g.8444_8447delinsCTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301691.3:c.639_642delinsCTAG MANE Select	ENSP00000301691.1:p.Tyr213=
ENST00000301691.2:c.639_642delinsCTAG	ENSP00000301691.1:p.Tyr213=
NM_025237.2:c.639_642delinsCTAG	NP_079513.1:p.Tyr213=
NM_025237.3:c.639_642delinsCTAG MANE Select	NP_079513.1:p.Tyr213=