Canonical Allele Identifier: CA471507930
Gene: SHOC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110964679_110964680insGGTTCTTTTTC , CM000672.2:g.110964679_110964680insGGTTCTTTTTC GRCh38
NC_000010.10:g.112724437_112724438insGGTTCTTTTTC , CM000672.1:g.112724437_112724438insGGTTCTTTTTC GRCh37
NC_000010.9:g.112714427_112714428insGGTTCTTTTTC NCBI36
NG_028922.1:g.50137_50138insGGTTCTTTTTC , LRG_753:g.50137_50138insGGTTCTTTTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000265277.10:c.321_322insGGTTCTTTTTC ENSP00000265277.5:p.Ser108GlyfsTer19
ENST00000451838.2:c.-242-35736_-242-35735insGGTTCTTTTTC ENSP00000408275.2:n.-242-35736_-242-35735insGGTTCTTTTTC
ENST00000480155.2:n.557_558insGGTTCTTTTTC
ENST00000685059.1:c.321_322insGGTTCTTTTTC ENSP00000510210.1:p.Ser108GlyfsTer19
ENST00000685613.1:c.321_322insGGTTCTTTTTC ENSP00000510564.1:p.Ser108GlyfsTer19
ENST00000687592.1:n.620_621insGGTTCTTTTTC
ENST00000688928.1:c.321_322insGGTTCTTTTTC ENSP00000509273.1:p.Ser108GlyfsTer19
ENST00000689118.1:c.321_322insGGTTCTTTTTC ENSP00000510554.1:p.Ser108GlyfsTer19
ENST00000689300.1:c.321_322insGGTTCTTTTTC ENSP00000510639.1:p.Ser108GlyfsTer19
ENST00000689997.1:c.-380-20949_-380-20948insGGTTCTTTTTC ENSP00000510700.1:n.-380-20949_-380-20948insGGTTCTTTTTC
ENST00000691151.1:n.613_614insGGTTCTTTTTC
ENST00000691369.1:c.321_322insGGTTCTTTTTC ENSP00000509754.1:p.Ser108GlyfsTer19
ENST00000691441.1:c.321_322insGGTTCTTTTTC ENSP00000509686.1:p.Ser108GlyfsTer19
ENST00000691903.1:c.321_322insGGTTCTTTTTC ENSP00000510314.1:p.Ser108GlyfsTer19
ENST00000692776.1:c.321_322insGGTTCTTTTTC ENSP00000508524.1:p.Ser108GlyfsTer19
ENST00000369452.9:c.321_322insGGTTCTTTTTC MANE Select ENSP00000358464.5:p.Ser108GlyfsTer19
ENST00000265277.9:c.321_322insGGTTCTTTTTC ENSP00000265277.5:p.Ser108GlyfsTer19
ENST00000369452.8:c.321_322insGGTTCTTTTTC ENSP00000358464.4:p.Ser108GlyfsTer19
ENST00000489390.1:n.56-35736_56-35735insGGTTCTTTTTC
ENST00000489783.1:n.699_700insGGTTCTTTTTC
NM_001269039.1:c.321_322insGGTTCTTTTTC NP_001255968.1:p.Ser108GlyfsTer19
NM_007373.3:c.321_322insGGTTCTTTTTC , LRG_753t1:c.321_322insGGTTCTTTTTC NP_031399.2:p.Ser108GlyfsTer19
XM_011540216.1:c.-380-20949_-380-20948insGGTTCTTTTTC XP_011538518.1:n.-380-20949_-380-20948insGGTTCTTTTTC
NM_001269039.2:c.321_322insGGTTCTTTTTC NP_001255968.1:p.Ser108GlyfsTer19
NM_001324336.1:c.321_322insGGTTCTTTTTC NP_001311265.1:p.Ser108GlyfsTer19
NM_001324337.1:c.321_322insGGTTCTTTTTC NP_001311266.1:p.Ser108GlyfsTer19
NR_136749.1:n.116-20949_116-20948insGGTTCTTTTTC
NM_007373.4:c.321_322insGGTTCTTTTTC MANE Select NP_031399.2:p.Ser108GlyfsTer19
NM_001269039.3:c.321_322insGGTTCTTTTTC NP_001255968.1:p.Ser108GlyfsTer19
NM_001324336.2:c.321_322insGGTTCTTTTTC NP_001311265.1:p.Ser108GlyfsTer19
NM_001324337.2:c.321_322insGGTTCTTTTTC NP_001311266.1:p.Ser108GlyfsTer19
NR_136749.2:n.55-20949_55-20948insGGTTCTTTTTC