Canonical Allele Identifier: CA1662104471

Gene: RSPO3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.127134977A= , CM000668.2:g.127134977A=	GRCh38
NC_000006.11:g.127456122A= , CM000668.1:g.127456122A=	GRCh37
NC_000006.10:g.127497815A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356698.9:c.98-13671A= MANE Select	ENSP00000349131.4:n.98-13671A=
ENST00000650648.1:n.401+42339T=
ENST00000650684.1:n.473+42339T=
ENST00000650727.1:n.440+42339T=
ENST00000650777.1:n.473-9086T=
ENST00000650823.1:n.448+42339T=
ENST00000650841.1:n.441-38424T=
ENST00000650899.1:n.467+42339T=
ENST00000651038.1:n.471+42339T=
ENST00000651052.1:n.88+42339T=
ENST00000651110.1:n.424-13241T=
ENST00000651273.1:n.489+42339T=
ENST00000651338.1:n.471+42339T=
ENST00000651421.1:n.747-13241T=
ENST00000651607.1:n.473+42339T=
ENST00000651795.1:n.440+42339T=
ENST00000651850.1:n.489+42339T=
ENST00000651963.1:n.138+42339T=
ENST00000652330.1:n.464+42339T=
ENST00000652419.1:n.91+42339T=
ENST00000652459.1:n.434+42339T=
ENST00000652545.1:n.489+42339T=
ENST00000356698.8:c.98-13671A=	ENSP00000349131.4:n.98-13671A=
ENST00000368317.3:c.98-13671A=	ENSP00000357300.3:n.98-13671A=
ENST00000485757.1:n.143-13671A=
NM_032784.4:c.98-13671A=	NP_116173.2:n.98-13671A=
XR_942959.1:n.691-13241T=
XM_017011378.1:c.98-13671A=	XP_016866867.1:n.98-13671A=
XM_017011379.1:c.-110-13671A=	XP_016866868.1:n.-110-13671A=
NM_032784.5:c.98-13671A= MANE Select	NP_116173.2:n.98-13671A=