Canonical Allele Identifier: CA2789489513
Gene: SHOC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110964347G>A , CM000672.2:g.110964347G>A GRCh38
NC_000010.10:g.112724105G>A , CM000672.1:g.112724105G>A GRCh37
NC_000010.9:g.112714095G>A NCBI36
NG_028922.1:g.49805G>A , LRG_753:g.49805G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265277.10:c.-12G>A ENSP00000265277.5:n.-12G>A
ENST00000451838.2:c.-242-36068G>A ENSP00000408275.2:n.-242-36068G>A
ENST00000480155.2:n.225G>A
ENST00000685059.1:c.-12G>A ENSP00000510210.1:n.-12G>A
ENST00000685613.1:c.-12G>A ENSP00000510564.1:n.-12G>A
ENST00000687592.1:n.288G>A
ENST00000688928.1:c.-12G>A ENSP00000509273.1:n.-12G>A
ENST00000689118.1:c.-12G>A ENSP00000510554.1:n.-12G>A
ENST00000689300.1:c.-12G>A ENSP00000510639.1:n.-12G>A
ENST00000689997.1:c.-380-21281G>A ENSP00000510700.1:n.-380-21281G>A
ENST00000691151.1:n.281G>A
ENST00000691369.1:c.-12G>A ENSP00000509754.1:n.-12G>A
ENST00000691441.1:c.-12G>A ENSP00000509686.1:n.-12G>A
ENST00000691903.1:c.-12G>A ENSP00000510314.1:n.-12G>A
ENST00000692776.1:c.-12G>A ENSP00000508524.1:n.-12G>A
ENST00000369452.9:c.-12G>A MANE Select ENSP00000358464.5:n.-12G>A
ENST00000265277.9:c.-12G>A ENSP00000265277.5:n.-12G>A
ENST00000369452.8:c.-12G>A ENSP00000358464.4:n.-12G>A
ENST00000480155.1:n.473G>A
ENST00000489390.1:n.56-36068G>A
ENST00000489783.1:n.367G>A
NM_001269039.1:c.-12G>A NP_001255968.1:n.-12G>A
NM_007373.3:c.-12G>A , LRG_753t1:c.-12G>A NP_031399.2:n.-12G>A
XM_011540216.1:c.-380-21281G>A XP_011538518.1:n.-380-21281G>A
NM_001269039.2:c.-12G>A NP_001255968.1:n.-12G>A
NM_001324336.1:c.-12G>A NP_001311265.1:n.-12G>A
NM_001324337.1:c.-12G>A NP_001311266.1:n.-12G>A
NR_136749.1:n.116-21281G>A
NM_007373.4:c.-12G>A MANE Select NP_031399.2:n.-12G>A
NM_001269039.3:c.-12G>A NP_001255968.1:n.-12G>A
NM_001324336.2:c.-12G>A NP_001311265.1:n.-12G>A
NM_001324337.2:c.-12G>A NP_001311266.1:n.-12G>A
NR_136749.2:n.55-21281G>A
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