Canonical Allele Identifier: CA2610906555
Gene: SHOC2 HGNC NCBI

Linked Data

gnomAD v4: 10-110965065-A-ATTATGTAACCTCATTACGCT
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110965065_110965066insTTATGTAACCTCATTACGCT , CM000672.2:g.110965065_110965066insTTATGTAACCTCATTACGCT GRCh38
NC_000010.10:g.112724823_112724824insTTATGTAACCTCATTACGCT , CM000672.1:g.112724823_112724824insTTATGTAACCTCATTACGCT GRCh37
NC_000010.9:g.112714813_112714814insTTATGTAACCTCATTACGCT NCBI36
NG_028922.1:g.50523_50524insTTATGTAACCTCATTACGCT , LRG_753:g.50523_50524insTTATGTAACCTCATTACGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265277.10:c.703+4_703+5insTTATGTAACCTCATTACGCT ENSP00000265277.5:n.703+4_703+5insTTATGTAACCTCATTACGCT
ENST00000451838.2:c.-242-35350_-242-35349insTTATGTAACCTCATTACGCT ENSP00000408275.2:n.-242-35350_-242-35349insTTATGTAACCTCATTAC...
ENST00000480155.2:n.939+4_939+5insTTATGTAACCTCATTACGCT
ENST00000685059.1:c.703+4_703+5insTTATGTAACCTCATTACGCT ENSP00000510210.1:n.703+4_703+5insTTATGTAACCTCATTACGCT
ENST00000685613.1:c.703+4_703+5insTTATGTAACCTCATTACGCT ENSP00000510564.1:n.703+4_703+5insTTATGTAACCTCATTACGCT
ENST00000687592.1:n.1002+4_1002+5insTTATGTAACCTCATTACGCT
ENST00000688928.1:c.703+4_703+5insTTATGTAACCTCATTACGCT ENSP00000509273.1:n.703+4_703+5insTTATGTAACCTCATTACGCT
ENST00000689118.1:c.703+4_703+5insTTATGTAACCTCATTACGCT ENSP00000510554.1:n.703+4_703+5insTTATGTAACCTCATTACGCT
ENST00000689300.1:c.703+4_703+5insTTATGTAACCTCATTACGCT ENSP00000510639.1:n.703+4_703+5insTTATGTAACCTCATTACGCT
ENST00000689997.1:c.-380-20563_-380-20562insTTATGTAACCTCATTACGCT ENSP00000510700.1:n.-380-20563_-380-20562insTTATGTAACCTCATTAC...
ENST00000691151.1:n.999_1000insTTATGTAACCTCATTACGCT
ENST00000691369.1:c.703+4_703+5insTTATGTAACCTCATTACGCT ENSP00000509754.1:n.703+4_703+5insTTATGTAACCTCATTACGCT
ENST00000691441.1:c.703+4_703+5insTTATGTAACCTCATTACGCT ENSP00000509686.1:n.703+4_703+5insTTATGTAACCTCATTACGCT
ENST00000691903.1:c.703+4_703+5insTTATGTAACCTCATTACGCT ENSP00000510314.1:n.703+4_703+5insTTATGTAACCTCATTACGCT
ENST00000692776.1:c.703+4_703+5insTTATGTAACCTCATTACGCT ENSP00000508524.1:n.703+4_703+5insTTATGTAACCTCATTACGCT
ENST00000369452.9:c.703+4_703+5insTTATGTAACCTCATTACGCT MANE Select ENSP00000358464.5:n.703+4_703+5insTTATGTAACCTCATTACGCT
ENST00000265277.9:c.703+4_703+5insTTATGTAACCTCATTACGCT ENSP00000265277.5:n.703+4_703+5insTTATGTAACCTCATTACGCT
ENST00000369452.8:c.703+4_703+5insTTATGTAACCTCATTACGCT ENSP00000358464.4:n.703+4_703+5insTTATGTAACCTCATTACGCT
ENST00000451838.1:c.211+4_211+5insTTATGTAACCTCATTACGCT ENSP00000408275.1:n.211+4_211+5insTTATGTAACCTCATTACGCT
ENST00000489390.1:n.56-35350_56-35349insTTATGTAACCTCATTACGCT
ENST00000497305.1:n.30+4_30+5insTTATGTAACCTCATTACGCT
NM_001269039.1:c.703+4_703+5insTTATGTAACCTCATTACGCT NP_001255968.1:n.703+4_703+5insTTATGTAACCTCATTACGCT
NM_007373.3:c.703+4_703+5insTTATGTAACCTCATTACGCT , LRG_753t1:c.703+4_703+5insTTATGTAACCTCATTACGCT NP_031399.2:n.703+4_703+5insTTATGTAACCTCATTACGCT
XM_011540216.1:c.-380-20563_-380-20562insTTATGTAACCTCATTACGCT XP_011538518.1:n.-380-20563_-380-20562insTTATGTAACCTCATTACGCT...
NM_001269039.2:c.703+4_703+5insTTATGTAACCTCATTACGCT NP_001255968.1:n.703+4_703+5insTTATGTAACCTCATTACGCT
NM_001324336.1:c.703+4_703+5insTTATGTAACCTCATTACGCT NP_001311265.1:n.703+4_703+5insTTATGTAACCTCATTACGCT
NM_001324337.1:c.703+4_703+5insTTATGTAACCTCATTACGCT NP_001311266.1:n.703+4_703+5insTTATGTAACCTCATTACGCT
NR_136749.1:n.116-20563_116-20562insTTATGTAACCTCATTACGCT
NM_007373.4:c.703+4_703+5insTTATGTAACCTCATTACGCT MANE Select NP_031399.2:n.703+4_703+5insTTATGTAACCTCATTACGCT
NM_001269039.3:c.703+4_703+5insTTATGTAACCTCATTACGCT NP_001255968.1:n.703+4_703+5insTTATGTAACCTCATTACGCT
NM_001324336.2:c.703+4_703+5insTTATGTAACCTCATTACGCT NP_001311265.1:n.703+4_703+5insTTATGTAACCTCATTACGCT
NM_001324337.2:c.703+4_703+5insTTATGTAACCTCATTACGCT NP_001311266.1:n.703+4_703+5insTTATGTAACCTCATTACGCT
NR_136749.2:n.55-20563_55-20562insTTATGTAACCTCATTACGCT
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