Canonical Allele Identifier: CA1953557886
Gene: SPON1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13974716T= , CM000673.2:g.13974716T= GRCh38
NC_000011.9:g.13996263T= , CM000673.1:g.13996263T= GRCh37
NC_000011.8:g.13952839T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000576479.4:c.239-8131T= MANE Select ENSP00000460236.1:n.239-8131T=
ENST00000576479.3:c.239-8131T= ENSP00000460236.1:n.239-8131T=
NM_006108.3:c.239-8131T= NP_006099.2:n.239-8131T=
NM_006108.4:c.239-8131T= MANE Select NP_006099.2:n.239-8131T=