Canonical Allele Identifier: CA2638110343
Gene: SOST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755862_43755863insCTGGAGACAGGCTTG , CM000679.2:g.43755862_43755863insCTGGAGACAGGCTTG GRCh38
NC_000017.10:g.41833230_41833231insCTGGAGACAGGCTTG , CM000679.1:g.41833230_41833231insCTGGAGACAGGCTTG GRCh37
NC_000017.9:g.39188756_39188757insCTGGAGACAGGCTTG NCBI36
NG_008078.2:g.7926_7927insCAAGCCTGTCTCCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-100_221-99insCAAGCCTGTCTCCAG MANE Select ENSP00000301691.1:n.221-100_221-99insCAAGCCTGTCTCCAG
ENST00000301691.2:c.221-100_221-99insCAAGCCTGTCTCCAG ENSP00000301691.1:n.221-100_221-99insCAAGCCTGTCTCCAG
NM_025237.2:c.221-100_221-99insCAAGCCTGTCTCCAG NP_079513.1:n.221-100_221-99insCAAGCCTGTCTCCAG
NM_025237.3:c.221-100_221-99insCAAGCCTGTCTCCAG MANE Select NP_079513.1:n.221-100_221-99insCAAGCCTGTCTCCAG