Canonical Allele Identifier: CA2789489588
Gene: SHOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110965136_110965137insCCAAACACACCCAACAC , CM000672.2:g.110965136_110965137insCCAAACACACCCAACAC GRCh38
NC_000010.10:g.112724894_112724895insCCAAACACACCCAACAC , CM000672.1:g.112724894_112724895insCCAAACACACCCAACAC GRCh37
NC_000010.9:g.112714884_112714885insCCAAACACACCCAACAC NCBI36
NG_028922.1:g.50594_50595insCCAAACACACCCAACAC , LRG_753:g.50594_50595insCCAAACACACCCAACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000265277.10:c.703+75_703+76insCCAAACACACCCAACAC ENSP00000265277.5:n.703+75_703+76insCCAAACACACCCAACAC
ENST00000451838.2:c.-242-35279_-242-35278insCCAAACACACCCAACAC ENSP00000408275.2:n.-242-35279_-242-35278insCCAAACACACCCAACAC...
ENST00000480155.2:n.939+75_939+76insCCAAACACACCCAACAC
ENST00000685059.1:c.703+75_703+76insCCAAACACACCCAACAC ENSP00000510210.1:n.703+75_703+76insCCAAACACACCCAACAC
ENST00000685613.1:c.703+75_703+76insCCAAACACACCCAACAC ENSP00000510564.1:n.703+75_703+76insCCAAACACACCCAACAC
ENST00000687592.1:n.1002+75_1002+76insCCAAACACACCCAACAC
ENST00000688928.1:c.703+75_703+76insCCAAACACACCCAACAC ENSP00000509273.1:n.703+75_703+76insCCAAACACACCCAACAC
ENST00000689118.1:c.703+75_703+76insCCAAACACACCCAACAC ENSP00000510554.1:n.703+75_703+76insCCAAACACACCCAACAC
ENST00000689300.1:c.703+75_703+76insCCAAACACACCCAACAC ENSP00000510639.1:n.703+75_703+76insCCAAACACACCCAACAC
ENST00000689997.1:c.-380-20492_-380-20491insCCAAACACACCCAACAC ENSP00000510700.1:n.-380-20492_-380-20491insCCAAACACACCCAACAC...
ENST00000691151.1:n.1070_1071insCCAAACACACCCAACAC
ENST00000691369.1:c.703+75_703+76insCCAAACACACCCAACAC ENSP00000509754.1:n.703+75_703+76insCCAAACACACCCAACAC
ENST00000691441.1:c.703+75_703+76insCCAAACACACCCAACAC ENSP00000509686.1:n.703+75_703+76insCCAAACACACCCAACAC
ENST00000691903.1:c.703+75_703+76insCCAAACACACCCAACAC ENSP00000510314.1:n.703+75_703+76insCCAAACACACCCAACAC
ENST00000692776.1:c.703+75_703+76insCCAAACACACCCAACAC ENSP00000508524.1:n.703+75_703+76insCCAAACACACCCAACAC
ENST00000369452.9:c.703+75_703+76insCCAAACACACCCAACAC MANE Select ENSP00000358464.5:n.703+75_703+76insCCAAACACACCCAACAC
ENST00000265277.9:c.703+75_703+76insCCAAACACACCCAACAC ENSP00000265277.5:n.703+75_703+76insCCAAACACACCCAACAC
ENST00000369452.8:c.703+75_703+76insCCAAACACACCCAACAC ENSP00000358464.4:n.703+75_703+76insCCAAACACACCCAACAC
ENST00000451838.1:c.211+75_211+76insCCAAACACACCCAACAC ENSP00000408275.1:n.211+75_211+76insCCAAACACACCCAACAC
ENST00000489390.1:n.56-35279_56-35278insCCAAACACACCCAACAC
ENST00000497305.1:n.30+75_30+76insCCAAACACACCCAACAC
NM_001269039.1:c.703+75_703+76insCCAAACACACCCAACAC NP_001255968.1:n.703+75_703+76insCCAAACACACCCAACAC
NM_007373.3:c.703+75_703+76insCCAAACACACCCAACAC , LRG_753t1:c.703+75_703+76insCCAAACACACCCAACAC NP_031399.2:n.703+75_703+76insCCAAACACACCCAACAC
XM_011540216.1:c.-380-20492_-380-20491insCCAAACACACCCAACAC XP_011538518.1:n.-380-20492_-380-20491insCCAAACACACCCAACAC
NM_001269039.2:c.703+75_703+76insCCAAACACACCCAACAC NP_001255968.1:n.703+75_703+76insCCAAACACACCCAACAC
NM_001324336.1:c.703+75_703+76insCCAAACACACCCAACAC NP_001311265.1:n.703+75_703+76insCCAAACACACCCAACAC
NM_001324337.1:c.703+75_703+76insCCAAACACACCCAACAC NP_001311266.1:n.703+75_703+76insCCAAACACACCCAACAC
NR_136749.1:n.116-20492_116-20491insCCAAACACACCCAACAC
NM_007373.4:c.703+75_703+76insCCAAACACACCCAACAC MANE Select NP_031399.2:n.703+75_703+76insCCAAACACACCCAACAC
NM_001269039.3:c.703+75_703+76insCCAAACACACCCAACAC NP_001255968.1:n.703+75_703+76insCCAAACACACCCAACAC
NM_001324336.2:c.703+75_703+76insCCAAACACACCCAACAC NP_001311265.1:n.703+75_703+76insCCAAACACACCCAACAC
NM_001324337.2:c.703+75_703+76insCCAAACACACCCAACAC NP_001311266.1:n.703+75_703+76insCCAAACACACCCAACAC
NR_136749.2:n.55-20492_55-20491insCCAAACACACCCAACAC