Canonical Allele Identifier: CA2610905963

Gene: SHOC2

Linked Data

• gnomAD v4: 10-110964317-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110964317A>C , CM000672.2:g.110964317A>C	GRCh38
NC_000010.10:g.112724075A>C , CM000672.1:g.112724075A>C	GRCh37
NC_000010.9:g.112714065A>C	NCBI36
NG_028922.1:g.49775A>C , LRG_753:g.49775A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265277.10:c.-42A>C	ENSP00000265277.5:n.-42A>C
ENST00000451838.2:c.-242-36098A>C	ENSP00000408275.2:n.-242-36098A>C
ENST00000480155.2:n.195A>C
ENST00000685059.1:c.-42A>C	ENSP00000510210.1:n.-42A>C
ENST00000685613.1:c.-42A>C	ENSP00000510564.1:n.-42A>C
ENST00000687592.1:n.258A>C
ENST00000688928.1:c.-42A>C	ENSP00000509273.1:n.-42A>C
ENST00000689118.1:c.-42A>C	ENSP00000510554.1:n.-42A>C
ENST00000689300.1:c.-42A>C	ENSP00000510639.1:n.-42A>C
ENST00000689997.1:c.-380-21311A>C	ENSP00000510700.1:n.-380-21311A>C
ENST00000691151.1:n.251A>C
ENST00000691369.1:c.-42A>C	ENSP00000509754.1:n.-42A>C
ENST00000691441.1:c.-42A>C	ENSP00000509686.1:n.-42A>C
ENST00000691903.1:c.-42A>C	ENSP00000510314.1:n.-42A>C
ENST00000692776.1:c.-42A>C	ENSP00000508524.1:n.-42A>C
ENST00000369452.9:c.-42A>C MANE Select	ENSP00000358464.5:n.-42A>C
ENST00000265277.9:c.-42A>C	ENSP00000265277.5:n.-42A>C
ENST00000369452.8:c.-42A>C	ENSP00000358464.4:n.-42A>C
ENST00000480155.1:n.443A>C
ENST00000489390.1:n.56-36098A>C
ENST00000489783.1:n.337A>C
NM_001269039.1:c.-42A>C	NP_001255968.1:n.-42A>C
NM_007373.3:c.-42A>C , LRG_753t1:c.-42A>C	NP_031399.2:n.-42A>C
XM_011540216.1:c.-380-21311A>C	XP_011538518.1:n.-380-21311A>C
NM_001269039.2:c.-42A>C	NP_001255968.1:n.-42A>C
NM_001324336.1:c.-42A>C	NP_001311265.1:n.-42A>C
NM_001324337.1:c.-42A>C	NP_001311266.1:n.-42A>C
NR_136749.1:n.116-21311A>C
NM_007373.4:c.-42A>C MANE Select	NP_031399.2:n.-42A>C
NM_001269039.3:c.-42A>C	NP_001255968.1:n.-42A>C
NM_001324336.2:c.-42A>C	NP_001311265.1:n.-42A>C
NM_001324337.2:c.-42A>C	NP_001311266.1:n.-42A>C
NR_136749.2:n.55-21311A>C