Canonical Allele Identifier: CA932534464
Gene: SHOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1847629235

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110964317_110964322dup , CM000672.2:g.110964317_110964322dup GRCh38
NC_000010.10:g.112724075_112724080dup , CM000672.1:g.112724075_112724080dup GRCh37
NC_000010.9:g.112714065_112714070dup NCBI36
NG_028922.1:g.49775_49780dup , LRG_753:g.49775_49780dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000265277.10:c.-42_-37dup ENSP00000265277.5:n.-42_-37dup
ENST00000451838.2:c.-242-36098_-242-36093dup ENSP00000408275.2:n.-242-36098_-242-36093dup
ENST00000480155.2:n.195_200dup
ENST00000685059.1:c.-42_-37dup ENSP00000510210.1:n.-42_-37dup
ENST00000685613.1:c.-42_-37dup ENSP00000510564.1:n.-42_-37dup
ENST00000687592.1:n.258_263dup
ENST00000688928.1:c.-42_-37dup ENSP00000509273.1:n.-42_-37dup
ENST00000689118.1:c.-42_-37dup ENSP00000510554.1:n.-42_-37dup
ENST00000689300.1:c.-42_-37dup ENSP00000510639.1:n.-42_-37dup
ENST00000689997.1:c.-380-21311_-380-21306dup ENSP00000510700.1:n.-380-21311_-380-21306dup
ENST00000691151.1:n.251_256dup
ENST00000691369.1:c.-42_-37dup ENSP00000509754.1:n.-42_-37dup
ENST00000691441.1:c.-42_-37dup ENSP00000509686.1:n.-42_-37dup
ENST00000691903.1:c.-42_-37dup ENSP00000510314.1:n.-42_-37dup
ENST00000692776.1:c.-42_-37dup ENSP00000508524.1:n.-42_-37dup
ENST00000369452.9:c.-42_-37dup MANE Select ENSP00000358464.5:n.-42_-37dup
ENST00000265277.9:c.-42_-37dup ENSP00000265277.5:n.-42_-37dup
ENST00000369452.8:c.-42_-37dup ENSP00000358464.4:n.-42_-37dup
ENST00000480155.1:n.443_448dup
ENST00000489390.1:n.56-36098_56-36093dup
ENST00000489783.1:n.337_342dup
NM_001269039.1:c.-42_-37dup NP_001255968.1:n.-42_-37dup
NM_007373.3:c.-42_-37dup , LRG_753t1:c.-42_-37dup NP_031399.2:n.-42_-37dup
XM_011540216.1:c.-380-21311_-380-21306dup XP_011538518.1:n.-380-21311_-380-21306dup
NM_001269039.2:c.-42_-37dup NP_001255968.1:n.-42_-37dup
NM_001324336.1:c.-42_-37dup NP_001311265.1:n.-42_-37dup
NM_001324337.1:c.-42_-37dup NP_001311266.1:n.-42_-37dup
NR_136749.1:n.116-21311_116-21306dup
NM_007373.4:c.-42_-37dup MANE Select NP_031399.2:n.-42_-37dup
NM_001269039.3:c.-42_-37dup NP_001255968.1:n.-42_-37dup
NM_001324336.2:c.-42_-37dup NP_001311265.1:n.-42_-37dup
NM_001324337.2:c.-42_-37dup NP_001311266.1:n.-42_-37dup
NR_136749.2:n.55-21311_55-21306dup