Canonical Allele Identifier: CA15477360
Gene: RSPO3 HGNC NCBI

Linked Data

dbSNP Id: rs7745274

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.127188012G>A , CM000668.2:g.127188012G>A GRCh38
NC_000006.11:g.127509157G>A , CM000668.1:g.127509157G>A GRCh37
NC_000006.10:g.127550850G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356698.9:c.635-7811G>A MANE Select ENSP00000349131.4:n.635-7811G>A
ENST00000650648.1:n.25-8016C>T
ENST00000650684.1:n.97-8016C>T
ENST00000650727.1:n.64-8016C>T
ENST00000650777.1:n.96-8016C>T
ENST00000650823.1:n.72-8016C>T
ENST00000650841.1:n.64-8016C>T
ENST00000650899.1:n.91-8016C>T
ENST00000651038.1:n.95-8016C>T
ENST00000651110.1:n.47-8016C>T
ENST00000651195.1:n.91-8016C>T
ENST00000651273.1:n.113-8016C>T
ENST00000651331.1:n.113-8016C>T
ENST00000651338.1:n.95-8016C>T
ENST00000651421.1:n.370-8016C>T
ENST00000651607.1:n.97-8016C>T
ENST00000651795.1:n.64-8016C>T
ENST00000651850.1:n.113-8016C>T
ENST00000652330.1:n.88-8016C>T
ENST00000652459.1:n.58-8016C>T
ENST00000652545.1:n.113-8016C>T
ENST00000356698.8:c.635-7811G>A ENSP00000349131.4:n.635-7811G>A
ENST00000368317.3:c.635-7811G>A ENSP00000357300.3:n.635-7811G>A
NM_032784.4:c.635-7811G>A NP_116173.2:n.635-7811G>A
XM_017011378.1:c.635-4632G>A XP_016866867.1:n.635-4632G>A
XM_017011379.1:c.428-7811G>A XP_016866868.1:n.428-7811G>A
XR_002956392.1:n.431-8016C>T
NM_032784.5:c.635-7811G>A MANE Select NP_116173.2:n.635-7811G>A