Canonical Allele Identifier: CA2610905547

Gene: SHOC2

Linked Data

• gnomAD v4: 10-110964073-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110964073A>C , CM000672.2:g.110964073A>C	GRCh38
NC_000010.10:g.112723831A>C , CM000672.1:g.112723831A>C	GRCh37
NC_000010.9:g.112713821A>C	NCBI36
NG_028922.1:g.49531A>C , LRG_753:g.49531A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265277.10:c.-234-52A>C	ENSP00000265277.5:n.-234-52A>C
ENST00000451838.2:c.-242-36342A>C	ENSP00000408275.2:n.-242-36342A>C
ENST00000480155.2:n.3-52A>C
ENST00000685059.1:c.-234-52A>C	ENSP00000510210.1:n.-234-52A>C
ENST00000685613.1:c.-234-52A>C	ENSP00000510564.1:n.-234-52A>C
ENST00000687592.1:n.66-52A>C
ENST00000688928.1:c.-234-52A>C	ENSP00000509273.1:n.-234-52A>C
ENST00000689118.1:c.-234-52A>C	ENSP00000510554.1:n.-234-52A>C
ENST00000689300.1:c.-234-52A>C	ENSP00000510639.1:n.-234-52A>C
ENST00000689997.1:c.-380-21555A>C	ENSP00000510700.1:n.-380-21555A>C
ENST00000691151.1:n.59-52A>C
ENST00000691369.1:c.-234-52A>C	ENSP00000509754.1:n.-234-52A>C
ENST00000691441.1:c.-234-52A>C	ENSP00000509686.1:n.-234-52A>C
ENST00000691903.1:c.-234-52A>C	ENSP00000510314.1:n.-234-52A>C
ENST00000692776.1:c.-234-52A>C	ENSP00000508524.1:n.-234-52A>C
ENST00000369452.9:c.-234-52A>C MANE Select	ENSP00000358464.5:n.-234-52A>C
ENST00000369452.8:c.-234-52A>C	ENSP00000358464.4:n.-234-52A>C
ENST00000480155.1:n.251-52A>C
ENST00000489390.1:n.56-36342A>C
ENST00000489783.1:n.145-52A>C
NM_007373.3:c.-234-52A>C , LRG_753t1:c.-234-52A>C	NP_031399.2:n.-234-52A>C
XM_011540216.1:c.-380-21555A>C	XP_011538518.1:n.-380-21555A>C
NM_001269039.2:c.-234-52A>C	NP_001255968.1:n.-234-52A>C
NM_001324336.1:c.-234-52A>C	NP_001311265.1:n.-234-52A>C
NM_001324337.1:c.-234-52A>C	NP_001311266.1:n.-234-52A>C
NR_136749.1:n.116-21555A>C
NM_007373.4:c.-234-52A>C MANE Select	NP_031399.2:n.-234-52A>C
NM_001269039.3:c.-234-52A>C	NP_001255968.1:n.-234-52A>C
NM_001324336.2:c.-234-52A>C	NP_001311265.1:n.-234-52A>C
NM_001324337.2:c.-234-52A>C	NP_001311266.1:n.-234-52A>C
NR_136749.2:n.55-21555A>C