Canonical Allele Identifier: CA645596160
Gene: SOST HGNC NCBI

Linked Data

COSMIC: COSM6147000
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755526_43755527delinsAT , CM000679.2:g.43755526_43755527delinsAT GRCh38
NC_000017.10:g.41832894_41832895delinsAT , CM000679.1:g.41832894_41832895delinsAT GRCh37
NC_000017.9:g.39188420_39188421delinsAT NCBI36
NG_008078.2:g.8262_8263delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.457_458delinsAT MANE Select ENSP00000301691.1:p.Ala153Met
ENST00000301691.2:c.457_458delinsAT ENSP00000301691.1:p.Ala153Met
NM_025237.2:c.457_458delinsAT NP_079513.1:p.Ala153Met
NM_025237.3:c.457_458delinsAT MANE Select NP_079513.1:p.Ala153Met
Search 100 bp 5'
Search 100 bp 3'