Canonical Allele Identifier: CA10634679

Gene: SHOC2

Linked Data

• ClinVar Variation Id: 298865
• ClinVar RCV Id: RCV000400784
• dbSNP Id: rs191293913
• gnomAD v2: 10-112771740-T-A
• gnomAD v3: 10-111011982-T-A
• gnomAD v4: 10-111011982-T-A
• MyVariant Identifiers: chr10:g.112771740T>A (hg19) ; chr10:g.111011982T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.111011982T>A , CM000672.2:g.111011982T>A	GRCh38
NC_000010.10:g.112771740T>A , CM000672.1:g.112771740T>A	GRCh37
NC_000010.9:g.112761730T>A	NCBI36
NG_028922.1:g.97440T>A , LRG_753:g.97440T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265277.10:c.*164T>A	ENSP00000265277.5:n.*164T>A
ENST00000451838.2:c.*164T>A	ENSP00000408275.2:n.*164T>A
ENST00000685059.1:c.*164T>A	ENSP00000510210.1:n.*164T>A
ENST00000685613.1:c.*909T>A	ENSP00000510564.1:n.*909T>A
ENST00000688928.1:c.*164T>A	ENSP00000509273.1:n.*164T>A
ENST00000689118.1:c.*164T>A	ENSP00000510554.1:n.*164T>A
ENST00000689300.1:c.*164T>A	ENSP00000510639.1:n.*164T>A
ENST00000689997.1:c.*164T>A	ENSP00000510700.1:n.*164T>A
ENST00000691369.1:c.*164T>A	ENSP00000509754.1:n.*164T>A
ENST00000691441.1:c.*164T>A	ENSP00000509686.1:n.*164T>A
ENST00000691903.1:c.*355T>A	ENSP00000510314.1:n.*355T>A
ENST00000369452.9:c.*164T>A MANE Select	ENSP00000358464.5:n.*164T>A
ENST00000265277.9:c.*164T>A	ENSP00000265277.5:n.*164T>A
ENST00000369452.8:c.*164T>A	ENSP00000358464.4:n.*164T>A
ENST00000451838.1:c.1283T>A	ENSP00000408275.1:n.1283T>A
NM_001269039.1:c.*164T>A	NP_001255968.1:n.*164T>A
NM_007373.3:c.*164T>A , LRG_753t1:c.*164T>A	NP_031399.2:n.*164T>A
XM_011540216.1:c.*164T>A	XP_011538518.1:n.*164T>A
NM_001269039.2:c.*164T>A	NP_001255968.1:n.*164T>A
NM_001324336.1:c.*164T>A	NP_001311265.1:n.*164T>A
NM_001324337.1:c.*164T>A	NP_001311266.1:n.*164T>A
NR_136749.1:n.1325T>A
NM_007373.4:c.*164T>A MANE Select	NP_031399.2:n.*164T>A
NM_001269039.3:c.*164T>A	NP_001255968.1:n.*164T>A
NM_001324336.2:c.*164T>A	NP_001311265.1:n.*164T>A
NM_001324337.2:c.*164T>A	NP_001311266.1:n.*164T>A
NR_136749.2:n.1264T>A