Canonical Allele Identifier: CA932534696
Gene: SHOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1847649128

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110965147_110965150del , CM000672.2:g.110965147_110965150del GRCh38
NC_000010.10:g.112724905_112724908del , CM000672.1:g.112724905_112724908del GRCh37
NC_000010.9:g.112714895_112714898del NCBI36
NG_028922.1:g.50605_50608del , LRG_753:g.50605_50608del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265277.10:c.703+86_703+89del ENSP00000265277.5:n.703+86_703+89del
ENST00000451838.2:c.-242-35268_-242-35265del ENSP00000408275.2:n.-242-35268_-242-35265del
ENST00000480155.2:n.939+86_939+89del
ENST00000685059.1:c.703+86_703+89del ENSP00000510210.1:n.703+86_703+89del
ENST00000685613.1:c.703+86_703+89del ENSP00000510564.1:n.703+86_703+89del
ENST00000687592.1:n.1002+86_1002+89del
ENST00000688928.1:c.703+86_703+89del ENSP00000509273.1:n.703+86_703+89del
ENST00000689118.1:c.703+86_703+89del ENSP00000510554.1:n.703+86_703+89del
ENST00000689300.1:c.703+86_703+89del ENSP00000510639.1:n.703+86_703+89del
ENST00000689997.1:c.-380-20481_-380-20478del ENSP00000510700.1:n.-380-20481_-380-20478del
ENST00000691151.1:n.1081_1084del
ENST00000691369.1:c.703+86_703+89del ENSP00000509754.1:n.703+86_703+89del
ENST00000691441.1:c.703+86_703+89del ENSP00000509686.1:n.703+86_703+89del
ENST00000691903.1:c.703+86_703+89del ENSP00000510314.1:n.703+86_703+89del
ENST00000692776.1:c.703+86_703+89del ENSP00000508524.1:n.703+86_703+89del
ENST00000369452.9:c.703+86_703+89del MANE Select ENSP00000358464.5:n.703+86_703+89del
ENST00000265277.9:c.703+86_703+89del ENSP00000265277.5:n.703+86_703+89del
ENST00000369452.8:c.703+86_703+89del ENSP00000358464.4:n.703+86_703+89del
ENST00000451838.1:c.211+86_211+89del ENSP00000408275.1:n.211+86_211+89del
ENST00000489390.1:n.56-35268_56-35265del
ENST00000497305.1:n.30+86_30+89del
NM_001269039.1:c.703+86_703+89del NP_001255968.1:n.703+86_703+89del
NM_007373.3:c.703+86_703+89del , LRG_753t1:c.703+86_703+89del NP_031399.2:n.703+86_703+89del
XM_011540216.1:c.-380-20481_-380-20478del XP_011538518.1:n.-380-20481_-380-20478del
NM_001269039.2:c.703+86_703+89del NP_001255968.1:n.703+86_703+89del
NM_001324336.1:c.703+86_703+89del NP_001311265.1:n.703+86_703+89del
NM_001324337.1:c.703+86_703+89del NP_001311266.1:n.703+86_703+89del
NR_136749.1:n.116-20481_116-20478del
NM_007373.4:c.703+86_703+89del MANE Select NP_031399.2:n.703+86_703+89del
NM_001269039.3:c.703+86_703+89del NP_001255968.1:n.703+86_703+89del
NM_001324336.2:c.703+86_703+89del NP_001311265.1:n.703+86_703+89del
NM_001324337.2:c.703+86_703+89del NP_001311266.1:n.703+86_703+89del
NR_136749.2:n.55-20481_55-20478del