Canonical Allele Identifier: CA454034038
Gene: SOSTDC1 HGNC NCBI
CRPPA HGNC NCBI

Linked Data

dbSNP Id: rs1387690638

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.16463528_16463530del , CM000669.2:g.16463528_16463530del GRCh38
NC_000007.13:g.16503153_16503155del , CM000669.1:g.16503153_16503155del GRCh37
NC_000007.12:g.16469678_16469680del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000307068.5:c.206-564_206-562del (SOSTDC1) MANE Select ENSP00000304930.4:n.206-564_206-562del
ENST00000674759.1:c.-47+32853_-47+32855del (CRPPA) ENSP00000502749.1:n.-47+32853_-47+32855del
ENST00000675257.1:c.-47+32853_-47+32855del (CRPPA) ENSP00000501664.1:n.-47+32853_-47+32855del
ENST00000307068.4:c.206-564_206-562del (SOSTDC1) ENSP00000304930.4:n.206-564_206-562del
ENST00000396652.1:c.278-564_278-562del (SOSTDC1) ENSP00000379889.1:n.278-564_278-562del
NM_015464.2:c.206-564_206-562del (SOSTDC1) NP_056279.1:n.206-564_206-562del
XM_011515502.1:c.-47+32853_-47+32855del (CRPPA) XP_011513804.1:n.-47+32853_-47+32855del
XM_011515503.1:c.-47+32853_-47+32855del (CRPPA) XP_011513805.1:n.-47+32853_-47+32855del
XM_011515504.1:c.-47+32853_-47+32855del (CRPPA) XP_011513806.1:n.-47+32853_-47+32855del
XM_011515505.1:c.-47+32853_-47+32855del (CRPPA) XP_011513807.1:n.-47+32853_-47+32855del
XM_011515506.1:c.-47+32853_-47+32855del (CRPPA) XP_011513808.1:n.-47+32853_-47+32855del
XM_011515507.1:c.-47+32853_-47+32855del (CRPPA) XP_011513809.1:n.-47+32853_-47+32855del
XR_927059.1:n.1117+2212_1117+2214del
XM_024446909.1:c.-47+32853_-47+32855del (CRPPA) XP_024302677.1:n.-47+32853_-47+32855del
XM_024446910.1:c.-47+32853_-47+32855del (CRPPA) XP_024302678.1:n.-47+32853_-47+32855del
XM_024446911.1:c.-47+32853_-47+32855del (CRPPA) XP_024302679.1:n.-47+32853_-47+32855del
XR_001745102.1:n.557_559del
NM_015464.3:c.206-564_206-562del (SOSTDC1) MANE Select NP_056279.1:n.206-564_206-562del