Canonical Allele Identifier: CA1662126896

Gene: RSPO3

Linked Data

• dbSNP Id: rs7745274

Genomic Alleles

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

Transcript Alleles

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