Canonical Allele Identifier: CA932534571
Gene: SHOC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110964662_110964663insTTT , CM000672.2:g.110964662_110964663insTTT GRCh38
NC_000010.10:g.112724420_112724421insTTT , CM000672.1:g.112724420_112724421insTTT GRCh37
NC_000010.9:g.112714410_112714411insTTT NCBI36
NG_028922.1:g.50120_50121insTTT , LRG_753:g.50120_50121insTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265277.10:c.304_305insTTT ENSP00000265277.5:p.Asn101_Ser102insPhe
ENST00000451838.2:c.-242-35753_-242-35752insTTT ENSP00000408275.2:n.-242-35753_-242-35752insTTT
ENST00000480155.2:n.540_541insTTT
ENST00000685059.1:c.304_305insTTT ENSP00000510210.1:p.Asn101_Ser102insPhe
ENST00000685613.1:c.304_305insTTT ENSP00000510564.1:p.Asn101_Ser102insPhe
ENST00000687592.1:n.603_604insTTT
ENST00000688928.1:c.304_305insTTT ENSP00000509273.1:p.Asn101_Ser102insPhe
ENST00000689118.1:c.304_305insTTT ENSP00000510554.1:p.Asn101_Ser102insPhe
ENST00000689300.1:c.304_305insTTT ENSP00000510639.1:p.Asn101_Ser102insPhe
ENST00000689997.1:c.-380-20966_-380-20965insTTT ENSP00000510700.1:n.-380-20966_-380-20965insTTT
ENST00000691151.1:n.596_597insTTT
ENST00000691369.1:c.304_305insTTT ENSP00000509754.1:p.Asn101_Ser102insPhe
ENST00000691441.1:c.304_305insTTT ENSP00000509686.1:p.Asn101_Ser102insPhe
ENST00000691903.1:c.304_305insTTT ENSP00000510314.1:p.Asn101_Ser102insPhe
ENST00000692776.1:c.304_305insTTT ENSP00000508524.1:p.Asn101_Ser102insPhe
ENST00000369452.9:c.304_305insTTT MANE Select ENSP00000358464.5:p.Asn101_Ser102insPhe
ENST00000265277.9:c.304_305insTTT ENSP00000265277.5:p.Asn101_Ser102insPhe
ENST00000369452.8:c.304_305insTTT ENSP00000358464.4:p.Asn101_Ser102insPhe
ENST00000489390.1:n.56-35753_56-35752insTTT
ENST00000489783.1:n.682_683insTTT
NM_001269039.1:c.304_305insTTT NP_001255968.1:p.Asn101_Ser102insPhe
NM_007373.3:c.304_305insTTT , LRG_753t1:c.304_305insTTT NP_031399.2:p.Asn101_Ser102insPhe
XM_011540216.1:c.-380-20966_-380-20965insTTT XP_011538518.1:n.-380-20966_-380-20965insTTT
NM_001269039.2:c.304_305insTTT NP_001255968.1:p.Asn101_Ser102insPhe
NM_001324336.1:c.304_305insTTT NP_001311265.1:p.Asn101_Ser102insPhe
NM_001324337.1:c.304_305insTTT NP_001311266.1:p.Asn101_Ser102insPhe
NR_136749.1:n.116-20966_116-20965insTTT
NM_007373.4:c.304_305insTTT MANE Select NP_031399.2:p.Asn101_Ser102insPhe
NM_001269039.3:c.304_305insTTT NP_001255968.1:p.Asn101_Ser102insPhe
NM_001324336.2:c.304_305insTTT NP_001311265.1:p.Asn101_Ser102insPhe
NM_001324337.2:c.304_305insTTT NP_001311266.1:p.Asn101_Ser102insPhe
NR_136749.2:n.55-20966_55-20965insTTT