Canonical Allele Identifier: CA2638110206
Gene: SOST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755367del , CM000679.2:g.43755367del GRCh38
NC_000017.10:g.41832735del , CM000679.1:g.41832735del GRCh37
NC_000017.9:g.39188261del NCBI36
NG_008078.2:g.8422del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.617del MANE Select ENSP00000301691.1:p.Gln206ArgfsTer?
ENST00000301691.2:c.617del ENSP00000301691.1:p.Gln206ArgfsTer?
NM_025237.2:c.617del NP_079513.1:p.Gln206ArgfsTer?
NM_025237.3:c.617del MANE Select NP_079513.1:p.Gln206ArgfsTer?