Canonical Allele Identifier: CA1690884064

Gene: SOSTDC1 CRPPA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.16463609G= , CM000669.2:g.16463609G=	GRCh38
NC_000007.13:g.16503234G= , CM000669.1:g.16503234G=	GRCh37
NC_000007.12:g.16469759G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307068.5:c.206-646C= (SOSTDC1) MANE Select	ENSP00000304930.4:n.206-646C=
ENST00000674759.1:c.-47+32771C= (CRPPA)	ENSP00000502749.1:n.-47+32771C=
ENST00000675257.1:c.-47+32771C= (CRPPA)	ENSP00000501664.1:n.-47+32771C=
ENST00000307068.4:c.206-646C= (SOSTDC1)	ENSP00000304930.4:n.206-646C=
ENST00000396652.1:c.278-646C= (SOSTDC1)	ENSP00000379889.1:n.278-646C=
NM_015464.2:c.206-646C= (SOSTDC1)	NP_056279.1:n.206-646C=
XM_011515502.1:c.-47+32771C= (CRPPA)	XP_011513804.1:n.-47+32771C=
XM_011515503.1:c.-47+32771C= (CRPPA)	XP_011513805.1:n.-47+32771C=
XM_011515504.1:c.-47+32771C= (CRPPA)	XP_011513806.1:n.-47+32771C=
XM_011515505.1:c.-47+32771C= (CRPPA)	XP_011513807.1:n.-47+32771C=
XM_011515506.1:c.-47+32771C= (CRPPA)	XP_011513808.1:n.-47+32771C=
XM_011515507.1:c.-47+32771C= (CRPPA)	XP_011513809.1:n.-47+32771C=
XR_927059.1:n.1117+2293G=
XM_024446909.1:c.-47+32771C= (CRPPA)	XP_024302677.1:n.-47+32771C=
XM_024446910.1:c.-47+32771C= (CRPPA)	XP_024302678.1:n.-47+32771C=
XM_024446911.1:c.-47+32771C= (CRPPA)	XP_024302679.1:n.-47+32771C=
XR_001745102.1:n.638G=
NM_015464.3:c.206-646C= (SOSTDC1) MANE Select	NP_056279.1:n.206-646C=