Canonical Allele Identifier: CA2610908398

Gene: SHOC2

Linked Data

• dbSNP Id: rs1848579157
• gnomAD v4: 10-111012206-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.111012206A>G , CM000672.2:g.111012206A>G	GRCh38
NC_000010.10:g.112771964A>G , CM000672.1:g.112771964A>G	GRCh37
NC_000010.9:g.112761954A>G	NCBI36
NG_028922.1:g.97664A>G , LRG_753:g.97664A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265277.10:c.*388A>G	ENSP00000265277.5:n.*388A>G
ENST00000451838.2:c.*388A>G	ENSP00000408275.2:n.*388A>G
ENST00000685059.1:c.*388A>G	ENSP00000510210.1:n.*388A>G
ENST00000685613.1:c.*1133A>G	ENSP00000510564.1:n.*1133A>G
ENST00000688928.1:c.*388A>G	ENSP00000509273.1:n.*388A>G
ENST00000689118.1:c.*388A>G	ENSP00000510554.1:n.*388A>G
ENST00000689300.1:c.*388A>G	ENSP00000510639.1:n.*388A>G
ENST00000689997.1:c.*388A>G	ENSP00000510700.1:n.*388A>G
ENST00000691369.1:c.*388A>G	ENSP00000509754.1:n.*388A>G
ENST00000691441.1:c.*388A>G	ENSP00000509686.1:n.*388A>G
ENST00000691903.1:c.*579A>G	ENSP00000510314.1:n.*579A>G
ENST00000369452.9:c.*388A>G MANE Select	ENSP00000358464.5:n.*388A>G
ENST00000265277.9:c.*388A>G	ENSP00000265277.5:n.*388A>G
ENST00000369452.8:c.*388A>G	ENSP00000358464.4:n.*388A>G
ENST00000451838.1:c.1507A>G	ENSP00000408275.1:n.1507A>G
NM_001269039.1:c.*388A>G	NP_001255968.1:n.*388A>G
NM_007373.3:c.*388A>G , LRG_753t1:c.*388A>G	NP_031399.2:n.*388A>G
XM_011540216.1:c.*388A>G	XP_011538518.1:n.*388A>G
NM_001269039.2:c.*388A>G	NP_001255968.1:n.*388A>G
NM_001324336.1:c.*388A>G	NP_001311265.1:n.*388A>G
NM_001324337.1:c.*388A>G	NP_001311266.1:n.*388A>G
NR_136749.1:n.1549A>G
NM_007373.4:c.*388A>G MANE Select	NP_031399.2:n.*388A>G
NM_001269039.3:c.*388A>G	NP_001255968.1:n.*388A>G
NM_001324336.2:c.*388A>G	NP_001311265.1:n.*388A>G
NM_001324337.2:c.*388A>G	NP_001311266.1:n.*388A>G
NR_136749.2:n.1488A>G