Canonical Allele Identifier: CA1139661685
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 917781
ClinVar RCV Id: RCV001175010
dbSNP Id: rs1847638431

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110964642_110964709dup , CM000672.2:g.110964642_110964709dup GRCh38
NC_000010.10:g.112724400_112724467dup , CM000672.1:g.112724400_112724467dup GRCh37
NC_000010.9:g.112714390_112714457dup NCBI36
NG_028922.1:g.50100_50167dup , LRG_753:g.50100_50167dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000265277.10:c.284_351dup ENSP00000265277.5:p.Ser118ThrfsTer28
ENST00000451838.2:c.-242-35773_-242-35706dup ENSP00000408275.2:n.-242-35773_-242-35706dup
ENST00000480155.2:n.520_587dup
ENST00000685059.1:c.284_351dup ENSP00000510210.1:p.Ser118ThrfsTer28
ENST00000685613.1:c.284_351dup ENSP00000510564.1:p.Ser118ThrfsTer28
ENST00000687592.1:n.583_650dup
ENST00000688928.1:c.284_351dup ENSP00000509273.1:p.Ser118ThrfsTer28
ENST00000689118.1:c.284_351dup ENSP00000510554.1:p.Ser118ThrfsTer28
ENST00000689300.1:c.284_351dup ENSP00000510639.1:p.Ser118ThrfsTer28
ENST00000689997.1:c.-380-20986_-380-20919dup ENSP00000510700.1:n.-380-20986_-380-20919dup
ENST00000691151.1:n.576_643dup
ENST00000691369.1:c.284_351dup ENSP00000509754.1:p.Ser118ThrfsTer28
ENST00000691441.1:c.284_351dup ENSP00000509686.1:p.Ser118ThrfsTer28
ENST00000691903.1:c.284_351dup ENSP00000510314.1:p.Ser118ThrfsTer28
ENST00000692776.1:c.284_351dup ENSP00000508524.1:p.Ser118ThrfsTer28
ENST00000369452.9:c.284_351dup MANE Select ENSP00000358464.5:p.Ser118ThrfsTer28
ENST00000265277.9:c.284_351dup ENSP00000265277.5:p.Ser118ThrfsTer28
ENST00000369452.8:c.284_351dup ENSP00000358464.4:p.Ser118ThrfsTer28
ENST00000489390.1:n.56-35773_56-35706dup
ENST00000489783.1:n.662_729dup
NM_001269039.1:c.284_351dup NP_001255968.1:p.Ser118ThrfsTer28
NM_007373.3:c.284_351dup , LRG_753t1:c.284_351dup NP_031399.2:p.Ser118ThrfsTer28
XM_011540216.1:c.-380-20986_-380-20919dup XP_011538518.1:n.-380-20986_-380-20919dup
NM_001269039.2:c.284_351dup NP_001255968.1:p.Ser118ThrfsTer28
NM_001324336.1:c.284_351dup NP_001311265.1:p.Ser118ThrfsTer28
NM_001324337.1:c.284_351dup NP_001311266.1:p.Ser118ThrfsTer28
NR_136749.1:n.116-20986_116-20919dup
NM_007373.4:c.284_351dup MANE Select NP_031399.2:p.Ser118ThrfsTer28
NM_001269039.3:c.284_351dup NP_001255968.1:p.Ser118ThrfsTer28
NM_001324336.2:c.284_351dup NP_001311265.1:p.Ser118ThrfsTer28
NM_001324337.2:c.284_351dup NP_001311266.1:p.Ser118ThrfsTer28
NR_136749.2:n.55-20986_55-20919dup