Canonical Allele Identifier: CA2610905844
Gene: SHOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1590804143

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110964251C>A , CM000672.2:g.110964251C>A GRCh38
NC_000010.10:g.112724009C>A , CM000672.1:g.112724009C>A GRCh37
NC_000010.9:g.112713999C>A NCBI36
NG_028922.1:g.49709C>A , LRG_753:g.49709C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265277.10:c.-108C>A ENSP00000265277.5:n.-108C>A
ENST00000451838.2:c.-242-36164C>A ENSP00000408275.2:n.-242-36164C>A
ENST00000480155.2:n.129C>A
ENST00000685059.1:c.-108C>A ENSP00000510210.1:n.-108C>A
ENST00000685613.1:c.-108C>A ENSP00000510564.1:n.-108C>A
ENST00000687592.1:n.192C>A
ENST00000688928.1:c.-108C>A ENSP00000509273.1:n.-108C>A
ENST00000689118.1:c.-108C>A ENSP00000510554.1:n.-108C>A
ENST00000689300.1:c.-108C>A ENSP00000510639.1:n.-108C>A
ENST00000689997.1:c.-380-21377C>A ENSP00000510700.1:n.-380-21377C>A
ENST00000691151.1:n.185C>A
ENST00000691369.1:c.-108C>A ENSP00000509754.1:n.-108C>A
ENST00000691441.1:c.-108C>A ENSP00000509686.1:n.-108C>A
ENST00000691903.1:c.-108C>A ENSP00000510314.1:n.-108C>A
ENST00000692776.1:c.-108C>A ENSP00000508524.1:n.-108C>A
ENST00000369452.9:c.-108C>A MANE Select ENSP00000358464.5:n.-108C>A
ENST00000265277.9:c.-108C>A ENSP00000265277.5:n.-108C>A
ENST00000369452.8:c.-108C>A ENSP00000358464.4:n.-108C>A
ENST00000480155.1:n.377C>A
ENST00000489390.1:n.56-36164C>A
ENST00000489783.1:n.271C>A
NM_001269039.1:c.-108C>A NP_001255968.1:n.-108C>A
NM_007373.3:c.-108C>A , LRG_753t1:c.-108C>A NP_031399.2:n.-108C>A
XM_011540216.1:c.-380-21377C>A XP_011538518.1:n.-380-21377C>A
NM_001269039.2:c.-108C>A NP_001255968.1:n.-108C>A
NM_001324336.1:c.-108C>A NP_001311265.1:n.-108C>A
NM_001324337.1:c.-108C>A NP_001311266.1:n.-108C>A
NR_136749.1:n.116-21377C>A
NM_007373.4:c.-108C>A MANE Select NP_031399.2:n.-108C>A
NM_001269039.3:c.-108C>A NP_001255968.1:n.-108C>A
NM_001324336.2:c.-108C>A NP_001311265.1:n.-108C>A
NM_001324337.2:c.-108C>A NP_001311266.1:n.-108C>A
NR_136749.2:n.55-21377C>A