Canonical Allele Identifier: CA10628065

Gene: SHOC2

Linked Data

• ClinVar Variation Id: 298878
• ClinVar RCV Id: RCV000327194
• dbSNP Id: rs886046735
• MyVariant Identifiers: chr10:g.112772794C>T (hg19) ; chr10:g.111013036C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.111013036C>T , CM000672.2:g.111013036C>T	GRCh38
NC_000010.10:g.112772794C>T , CM000672.1:g.112772794C>T	GRCh37
NC_000010.9:g.112762784C>T	NCBI36
NG_028922.1:g.98494C>T , LRG_753:g.98494C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265277.10:c.*1218C>T	ENSP00000265277.5:n.*1218C>T
ENST00000451838.2:c.*1218C>T	ENSP00000408275.2:n.*1218C>T
ENST00000685059.1:c.*1218C>T	ENSP00000510210.1:n.*1218C>T
ENST00000685613.1:c.*1963C>T	ENSP00000510564.1:n.*1963C>T
ENST00000688928.1:c.*1218C>T	ENSP00000509273.1:n.*1218C>T
ENST00000689118.1:c.*1218C>T	ENSP00000510554.1:n.*1218C>T
ENST00000689300.1:c.*1218C>T	ENSP00000510639.1:n.*1218C>T
ENST00000689997.1:c.*1218C>T	ENSP00000510700.1:n.*1218C>T
ENST00000691369.1:c.*1218C>T	ENSP00000509754.1:n.*1218C>T
ENST00000691441.1:c.*1218C>T	ENSP00000509686.1:n.*1218C>T
ENST00000691903.1:c.*1409C>T	ENSP00000510314.1:n.*1409C>T
ENST00000369452.9:c.*1218C>T MANE Select	ENSP00000358464.5:n.*1218C>T
ENST00000265277.9:c.*1218C>T	ENSP00000265277.5:n.*1218C>T
ENST00000369452.8:c.*1218C>T	ENSP00000358464.4:n.*1218C>T
ENST00000451838.1:c.2337C>T	ENSP00000408275.1:n.2337C>T
NM_001269039.1:c.*1218C>T	NP_001255968.1:n.*1218C>T
NM_007373.3:c.*1218C>T , LRG_753t1:c.*1218C>T	NP_031399.2:n.*1218C>T
XM_011540216.1:c.*1218C>T	XP_011538518.1:n.*1218C>T
NM_001269039.2:c.*1218C>T	NP_001255968.1:n.*1218C>T
NM_001324336.1:c.*1218C>T	NP_001311265.1:n.*1218C>T
NM_001324337.1:c.*1218C>T	NP_001311266.1:n.*1218C>T
NR_136749.1:n.2379C>T
NM_007373.4:c.*1218C>T MANE Select	NP_031399.2:n.*1218C>T
NM_001269039.3:c.*1218C>T	NP_001255968.1:n.*1218C>T
NM_001324336.2:c.*1218C>T	NP_001311265.1:n.*1218C>T
NM_001324337.2:c.*1218C>T	NP_001311266.1:n.*1218C>T
NR_136749.2:n.2318C>T