Canonical Allele Identifier: CA1953603937
Gene: SPON1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14076875T= , CM000673.2:g.14076875T= GRCh38
NC_000011.9:g.14098422T= , CM000673.1:g.14098422T= GRCh37
NC_000011.8:g.14054998T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000576479.4:c.553+1457T= MANE Select ENSP00000460236.1:n.553+1457T=
ENST00000576479.3:c.553+1457T= ENSP00000460236.1:n.553+1457T=
NM_006108.3:c.553+1457T= NP_006099.2:n.553+1457T=
NM_006108.4:c.553+1457T= MANE Select NP_006099.2:n.553+1457T=