Canonical Allele Identifier: CA399701115

Gene: SOST

Linked Data

• gnomAD v4: 17-43755344-A-G
• MyVariant Identifiers: chr17:g.41832712A>G (hg19) ; chr17:g.43755344A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43755344A>G , CM000679.2:g.43755344A>G	GRCh38
NC_000017.10:g.41832712A>G , CM000679.1:g.41832712A>G	GRCh37
NC_000017.9:g.39188238A>G	NCBI36
NG_008078.2:g.8445T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301691.3:c.640T>C MANE Select	ENSP00000301691.1:p.Ter214Gln
ENST00000301691.2:c.640T>C	ENSP00000301691.1:p.Ter214Gln
NM_025237.2:c.640T>C	NP_079513.1:p.Ter214Gln
NM_025237.3:c.640T>C MANE Select	NP_079513.1:p.Ter214Gln