Canonical Allele Identifier: CA15711636

Gene: SPON1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14138958G>A , CM000673.2:g.14138958G>A	GRCh38
NC_000011.9:g.14160504G>A , CM000673.1:g.14160504G>A	GRCh37
NC_000011.8:g.14117080G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576479.4:c.825+3390G>A MANE Select	ENSP00000460236.1:n.825+3390G>A
ENST00000576479.3:c.825+3390G>A	ENSP00000460236.1:n.825+3390G>A
NM_006108.3:c.825+3390G>A	NP_006099.2:n.825+3390G>A
NM_006108.4:c.825+3390G>A MANE Select	NP_006099.2:n.825+3390G>A