Canonical Allele Identifier: CA2497309233
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1030214
ClinVar RCV Id: RCV001331723
dbSNP Id: rs1847643137

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110964864_110964865delinsC , CM000672.2:g.110964864_110964865delinsC GRCh38
NC_000010.10:g.112724622_112724623delinsC , CM000672.1:g.112724622_112724623delinsC GRCh37
NC_000010.9:g.112714612_112714613delinsC NCBI36
NG_028922.1:g.50322_50323delinsC , LRG_753:g.50322_50323delinsC

Transcript Alleles

HGVS Amino-acid Change
ENST00000265277.10:c.506_507delinsC ENSP00000265277.5:p.Lys169ThrfsTer13
ENST00000451838.2:c.-242-35551_-242-35550delinsC ENSP00000408275.2:n.-242-35551_-242-35550delinsC
ENST00000480155.2:n.742_743delinsC
ENST00000685059.1:c.506_507delinsC ENSP00000510210.1:p.Lys169ThrfsTer13
ENST00000685613.1:c.506_507delinsC ENSP00000510564.1:p.Lys169ThrfsTer13
ENST00000687592.1:n.805_806delinsC
ENST00000688928.1:c.506_507delinsC ENSP00000509273.1:p.Lys169ThrfsTer13
ENST00000689118.1:c.506_507delinsC ENSP00000510554.1:p.Lys169ThrfsTer13
ENST00000689300.1:c.506_507delinsC ENSP00000510639.1:p.Lys169ThrfsTer13
ENST00000689997.1:c.-380-20764_-380-20763delinsC ENSP00000510700.1:n.-380-20764_-380-20763delinsC
ENST00000691151.1:n.798_799delinsC
ENST00000691369.1:c.506_507delinsC ENSP00000509754.1:p.Lys169ThrfsTer13
ENST00000691441.1:c.506_507delinsC ENSP00000509686.1:p.Lys169ThrfsTer13
ENST00000691903.1:c.506_507delinsC ENSP00000510314.1:p.Lys169ThrfsTer13
ENST00000692776.1:c.506_507delinsC ENSP00000508524.1:p.Lys169ThrfsTer13
ENST00000369452.9:c.506_507delinsC MANE Select ENSP00000358464.5:p.Lys169ThrfsTer13
ENST00000265277.9:c.506_507delinsC ENSP00000265277.5:p.Lys169ThrfsTer13
ENST00000369452.8:c.506_507delinsC ENSP00000358464.4:p.Lys169ThrfsTer13
ENST00000451838.1:c.14_15delinsC ENSP00000408275.1:p.Lys5ThrfsTer13
ENST00000489390.1:n.56-35551_56-35550delinsC
NM_001269039.1:c.506_507delinsC NP_001255968.1:p.Lys169ThrfsTer13
NM_007373.3:c.506_507delinsC , LRG_753t1:c.506_507delinsC NP_031399.2:p.Lys169ThrfsTer13
XM_011540216.1:c.-380-20764_-380-20763delinsC XP_011538518.1:n.-380-20764_-380-20763delinsC
NM_001269039.2:c.506_507delinsC NP_001255968.1:p.Lys169ThrfsTer13
NM_001324336.1:c.506_507delinsC NP_001311265.1:p.Lys169ThrfsTer13
NM_001324337.1:c.506_507delinsC NP_001311266.1:p.Lys169ThrfsTer13
NR_136749.1:n.116-20764_116-20763delinsC
NM_007373.4:c.506_507delinsC MANE Select NP_031399.2:p.Lys169ThrfsTer13
NM_001269039.3:c.506_507delinsC NP_001255968.1:p.Lys169ThrfsTer13
NM_001324336.2:c.506_507delinsC NP_001311265.1:p.Lys169ThrfsTer13
NM_001324337.2:c.506_507delinsC NP_001311266.1:p.Lys169ThrfsTer13
NR_136749.2:n.55-20764_55-20763delinsC