Canonical Allele Identifier: CA378386179
Gene: SHOC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110964945C>A , CM000672.2:g.110964945C>A GRCh38
NC_000010.10:g.112724703C>A , CM000672.1:g.112724703C>A GRCh37
NC_000010.9:g.112714693C>A NCBI36
NG_028922.1:g.50403C>A , LRG_753:g.50403C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265277.10:c.587C>A ENSP00000265277.5:p.Thr196Asn
ENST00000451838.2:c.-242-35470C>A ENSP00000408275.2:n.-242-35470C>A
ENST00000480155.2:n.823C>A
ENST00000685059.1:c.587C>A ENSP00000510210.1:p.Thr196Asn
ENST00000685613.1:c.587C>A ENSP00000510564.1:p.Thr196Asn
ENST00000687592.1:n.886C>A
ENST00000688928.1:c.587C>A ENSP00000509273.1:p.Thr196Asn
ENST00000689118.1:c.587C>A ENSP00000510554.1:p.Thr196Asn
ENST00000689300.1:c.587C>A ENSP00000510639.1:p.Thr196Asn
ENST00000689997.1:c.-380-20683C>A ENSP00000510700.1:n.-380-20683C>A
ENST00000691151.1:n.879C>A
ENST00000691369.1:c.587C>A ENSP00000509754.1:p.Thr196Asn
ENST00000691441.1:c.587C>A ENSP00000509686.1:p.Thr196Asn
ENST00000691903.1:c.587C>A ENSP00000510314.1:p.Thr196Asn
ENST00000692776.1:c.587C>A ENSP00000508524.1:p.Thr196Asn
ENST00000369452.9:c.587C>A MANE Select ENSP00000358464.5:p.Thr196Asn
ENST00000265277.9:c.587C>A ENSP00000265277.5:p.Thr196Asn
ENST00000369452.8:c.587C>A ENSP00000358464.4:p.Thr196Asn
ENST00000451838.1:c.95C>A ENSP00000408275.1:p.Thr32Asn
ENST00000489390.1:n.56-35470C>A
NM_001269039.1:c.587C>A NP_001255968.1:p.Thr196Asn
NM_007373.3:c.587C>A , LRG_753t1:c.587C>A NP_031399.2:p.Thr196Asn
XM_011540216.1:c.-380-20683C>A XP_011538518.1:n.-380-20683C>A
NM_001269039.2:c.587C>A NP_001255968.1:p.Thr196Asn
NM_001324336.1:c.587C>A NP_001311265.1:p.Thr196Asn
NM_001324337.1:c.587C>A NP_001311266.1:p.Thr196Asn
NR_136749.1:n.116-20683C>A
NM_007373.4:c.587C>A MANE Select NP_031399.2:p.Thr196Asn
NM_001269039.3:c.587C>A NP_001255968.1:p.Thr196Asn
NM_001324336.2:c.587C>A NP_001311265.1:p.Thr196Asn
NM_001324337.2:c.587C>A NP_001311266.1:p.Thr196Asn
NR_136749.2:n.55-20683C>A