Canonical Allele Identifier: CA2638110302
Gene: SOST HGNC NCBI

Linked Data

gnomAD v4: 17-43755822-GGCCCGTCTCTCTCCACCCCA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755827_43755846del , CM000679.2:g.43755827_43755846del GRCh38
NC_000017.10:g.41833195_41833214del , CM000679.1:g.41833195_41833214del GRCh37
NC_000017.9:g.39188721_39188740del NCBI36
NG_008078.2:g.7947_7966del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-79_221-60del MANE Select ENSP00000301691.1:n.221-79_221-60del
ENST00000301691.2:c.221-79_221-60del ENSP00000301691.1:n.221-79_221-60del
NM_025237.2:c.221-79_221-60del NP_079513.1:n.221-79_221-60del
NM_025237.3:c.221-79_221-60del MANE Select NP_079513.1:n.221-79_221-60del
Search 100 bp 5'
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