Canonical Allele Identifier: CA1953557779
Gene: SPON1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13974441A= , CM000673.2:g.13974441A= GRCh38
NC_000011.9:g.13995988A= , CM000673.1:g.13995988A= GRCh37
NC_000011.8:g.13952564A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000576479.4:c.239-8406A= MANE Select ENSP00000460236.1:n.239-8406A=
ENST00000576479.3:c.239-8406A= ENSP00000460236.1:n.239-8406A=
NM_006108.3:c.239-8406A= NP_006099.2:n.239-8406A=
NM_006108.4:c.239-8406A= MANE Select NP_006099.2:n.239-8406A=
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