Canonical Allele Identifier: CA399702473

Gene: SOST

Linked Data

• MyVariant Identifiers: chr17:g.41833099A>T (hg19) ; chr17:g.43755731A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43755731A>T , CM000679.2:g.43755731A>T	GRCh38
NC_000017.10:g.41833099A>T , CM000679.1:g.41833099A>T	GRCh37
NC_000017.9:g.39188625A>T	NCBI36
NG_008078.2:g.8058T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301691.3:c.253T>A MANE Select	ENSP00000301691.1:p.Phe85Ile
ENST00000301691.2:c.253T>A	ENSP00000301691.1:p.Phe85Ile
NM_025237.2:c.253T>A	NP_079513.1:p.Phe85Ile
NM_025237.3:c.253T>A MANE Select	NP_079513.1:p.Phe85Ile