Canonical Allele Identifier: CA932534582
Gene: SHOC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110964667_110964668insATA , CM000672.2:g.110964667_110964668insATA GRCh38
NC_000010.10:g.112724425_112724426insATA , CM000672.1:g.112724425_112724426insATA GRCh37
NC_000010.9:g.112714415_112714416insATA NCBI36
NG_028922.1:g.50125_50126insATA , LRG_753:g.50125_50126insATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000265277.10:c.309_310insATA ENSP00000265277.5:p.Met103_Arg104insIle
ENST00000451838.2:c.-242-35748_-242-35747insATA ENSP00000408275.2:n.-242-35748_-242-35747insATA
ENST00000480155.2:n.545_546insATA
ENST00000685059.1:c.309_310insATA ENSP00000510210.1:p.Met103_Arg104insIle
ENST00000685613.1:c.309_310insATA ENSP00000510564.1:p.Met103_Arg104insIle
ENST00000687592.1:n.608_609insATA
ENST00000688928.1:c.309_310insATA ENSP00000509273.1:p.Met103_Arg104insIle
ENST00000689118.1:c.309_310insATA ENSP00000510554.1:p.Met103_Arg104insIle
ENST00000689300.1:c.309_310insATA ENSP00000510639.1:p.Met103_Arg104insIle
ENST00000689997.1:c.-380-20961_-380-20960insATA ENSP00000510700.1:n.-380-20961_-380-20960insATA
ENST00000691151.1:n.601_602insATA
ENST00000691369.1:c.309_310insATA ENSP00000509754.1:p.Met103_Arg104insIle
ENST00000691441.1:c.309_310insATA ENSP00000509686.1:p.Met103_Arg104insIle
ENST00000691903.1:c.309_310insATA ENSP00000510314.1:p.Met103_Arg104insIle
ENST00000692776.1:c.309_310insATA ENSP00000508524.1:p.Met103_Arg104insIle
ENST00000369452.9:c.309_310insATA MANE Select ENSP00000358464.5:p.Met103_Arg104insIle
ENST00000265277.9:c.309_310insATA ENSP00000265277.5:p.Met103_Arg104insIle
ENST00000369452.8:c.309_310insATA ENSP00000358464.4:p.Met103_Arg104insIle
ENST00000489390.1:n.56-35748_56-35747insATA
ENST00000489783.1:n.687_688insATA
NM_001269039.1:c.309_310insATA NP_001255968.1:p.Met103_Arg104insIle
NM_007373.3:c.309_310insATA , LRG_753t1:c.309_310insATA NP_031399.2:p.Met103_Arg104insIle
XM_011540216.1:c.-380-20961_-380-20960insATA XP_011538518.1:n.-380-20961_-380-20960insATA
NM_001269039.2:c.309_310insATA NP_001255968.1:p.Met103_Arg104insIle
NM_001324336.1:c.309_310insATA NP_001311265.1:p.Met103_Arg104insIle
NM_001324337.1:c.309_310insATA NP_001311266.1:p.Met103_Arg104insIle
NR_136749.1:n.116-20961_116-20960insATA
NM_007373.4:c.309_310insATA MANE Select NP_031399.2:p.Met103_Arg104insIle
NM_001269039.3:c.309_310insATA NP_001255968.1:p.Met103_Arg104insIle
NM_001324336.2:c.309_310insATA NP_001311265.1:p.Met103_Arg104insIle
NM_001324337.2:c.309_310insATA NP_001311266.1:p.Met103_Arg104insIle
NR_136749.2:n.55-20961_55-20960insATA