Canonical Allele Identifier: CA2261069333
Gene: SOST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755803_43755806delinsGCCA , CM000679.2:g.43755803_43755806delinsGCCA GRCh38
NC_000017.10:g.41833171_41833174delinsGCCA , CM000679.1:g.41833171_41833174delinsGCCA GRCh37
NC_000017.9:g.39188697_39188700delinsGCCA NCBI36
NG_008078.2:g.7983_7986delinsTGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-43_221-40delinsTGGC MANE Select ENSP00000301691.1:n.221-43_221-40delinsTGGC
ENST00000301691.2:c.221-43_221-40delinsTGGC ENSP00000301691.1:n.221-43_221-40delinsTGGC
NM_025237.2:c.221-43_221-40delinsTGGC NP_079513.1:n.221-43_221-40delinsTGGC
NM_025237.3:c.221-43_221-40delinsTGGC MANE Select NP_079513.1:n.221-43_221-40delinsTGGC