Canonical Allele Identifier: CA2497309232
Gene: SHOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1847634645

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110964489_110964490insACTACTACTCATGGT , CM000672.2:g.110964489_110964490insACTACTACTCATGGT GRCh38
NC_000010.10:g.112724247_112724248insACTACTACTCATGGT , CM000672.1:g.112724247_112724248insACTACTACTCATGGT GRCh37
NC_000010.9:g.112714237_112714238insACTACTACTCATGGT NCBI36
NG_028922.1:g.49947_49948insACTACTACTCATGGT , LRG_753:g.49947_49948insACTACTACTCATGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265277.10:c.131_132insACTACTACTCATGGT ENSP00000265277.5:p.Lys44_Thr45insLeuLeuLeuMetVal
ENST00000451838.2:c.-242-35926_-242-35925insACTACTACTCATGGT ENSP00000408275.2:n.-242-35926_-242-35925insACTACTACTCATGGT
ENST00000480155.2:n.367_368insACTACTACTCATGGT
ENST00000685059.1:c.131_132insACTACTACTCATGGT ENSP00000510210.1:p.Lys44_Thr45insLeuLeuLeuMetVal
ENST00000685613.1:c.131_132insACTACTACTCATGGT ENSP00000510564.1:p.Lys44_Thr45insLeuLeuLeuMetVal
ENST00000687592.1:n.430_431insACTACTACTCATGGT
ENST00000688928.1:c.131_132insACTACTACTCATGGT ENSP00000509273.1:p.Lys44_Thr45insLeuLeuLeuMetVal
ENST00000689118.1:c.131_132insACTACTACTCATGGT ENSP00000510554.1:p.Lys44_Thr45insLeuLeuLeuMetVal
ENST00000689300.1:c.131_132insACTACTACTCATGGT ENSP00000510639.1:p.Lys44_Thr45insLeuLeuLeuMetVal
ENST00000689997.1:c.-380-21139_-380-21138insACTACTACTCATGGT ENSP00000510700.1:n.-380-21139_-380-21138insACTACTACTCATGGT
ENST00000691151.1:n.423_424insACTACTACTCATGGT
ENST00000691369.1:c.131_132insACTACTACTCATGGT ENSP00000509754.1:p.Lys44_Thr45insLeuLeuLeuMetVal
ENST00000691441.1:c.131_132insACTACTACTCATGGT ENSP00000509686.1:p.Lys44_Thr45insLeuLeuLeuMetVal
ENST00000691903.1:c.131_132insACTACTACTCATGGT ENSP00000510314.1:p.Lys44_Thr45insLeuLeuLeuMetVal
ENST00000692776.1:c.131_132insACTACTACTCATGGT ENSP00000508524.1:p.Lys44_Thr45insLeuLeuLeuMetVal
ENST00000369452.9:c.131_132insACTACTACTCATGGT MANE Select ENSP00000358464.5:p.Lys44_Thr45insLeuLeuLeuMetVal
ENST00000265277.9:c.131_132insACTACTACTCATGGT ENSP00000265277.5:p.Lys44_Thr45insLeuLeuLeuMetVal
ENST00000369452.8:c.131_132insACTACTACTCATGGT ENSP00000358464.4:p.Lys44_Thr45insLeuLeuLeuMetVal
ENST00000480155.1:n.615_616insACTACTACTCATGGT
ENST00000489390.1:n.56-35926_56-35925insACTACTACTCATGGT
ENST00000489783.1:n.509_510insACTACTACTCATGGT
NM_001269039.1:c.131_132insACTACTACTCATGGT NP_001255968.1:p.Lys44_Thr45insLeuLeuLeuMetVal
NM_007373.3:c.131_132insACTACTACTCATGGT , LRG_753t1:c.131_132insACTACTACTCATGGT NP_031399.2:p.Lys44_Thr45insLeuLeuLeuMetVal
XM_011540216.1:c.-380-21139_-380-21138insACTACTACTCATGGT XP_011538518.1:n.-380-21139_-380-21138insACTACTACTCATGGT
NM_001269039.2:c.131_132insACTACTACTCATGGT NP_001255968.1:p.Lys44_Thr45insLeuLeuLeuMetVal
NM_001324336.1:c.131_132insACTACTACTCATGGT NP_001311265.1:p.Lys44_Thr45insLeuLeuLeuMetVal
NM_001324337.1:c.131_132insACTACTACTCATGGT NP_001311266.1:p.Lys44_Thr45insLeuLeuLeuMetVal
NR_136749.1:n.116-21139_116-21138insACTACTACTCATGGT
NM_007373.4:c.131_132insACTACTACTCATGGT MANE Select NP_031399.2:p.Lys44_Thr45insLeuLeuLeuMetVal
NM_001269039.3:c.131_132insACTACTACTCATGGT NP_001255968.1:p.Lys44_Thr45insLeuLeuLeuMetVal
NM_001324336.2:c.131_132insACTACTACTCATGGT NP_001311265.1:p.Lys44_Thr45insLeuLeuLeuMetVal
NM_001324337.2:c.131_132insACTACTACTCATGGT NP_001311266.1:p.Lys44_Thr45insLeuLeuLeuMetVal
NR_136749.2:n.55-21139_55-21138insACTACTACTCATGGT