Canonical Allele Identifier: CA378385841

Gene: SHOC2

Linked Data

• MyVariant Identifiers: chr10:g.112724643T>G (hg19) ; chr10:g.110964885T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110964885T>G , CM000672.2:g.110964885T>G	GRCh38
NC_000010.10:g.112724643T>G , CM000672.1:g.112724643T>G	GRCh37
NC_000010.9:g.112714633T>G	NCBI36
NG_028922.1:g.50343T>G , LRG_753:g.50343T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265277.10:c.527T>G	ENSP00000265277.5:p.Leu176Ter
ENST00000451838.2:c.-242-35530T>G	ENSP00000408275.2:n.-242-35530T>G
ENST00000480155.2:n.763T>G
ENST00000685059.1:c.527T>G	ENSP00000510210.1:p.Leu176Ter
ENST00000685613.1:c.527T>G	ENSP00000510564.1:p.Leu176Ter
ENST00000687592.1:n.826T>G
ENST00000688928.1:c.527T>G	ENSP00000509273.1:p.Leu176Ter
ENST00000689118.1:c.527T>G	ENSP00000510554.1:p.Leu176Ter
ENST00000689300.1:c.527T>G	ENSP00000510639.1:p.Leu176Ter
ENST00000689997.1:c.-380-20743T>G	ENSP00000510700.1:n.-380-20743T>G
ENST00000691151.1:n.819T>G
ENST00000691369.1:c.527T>G	ENSP00000509754.1:p.Leu176Ter
ENST00000691441.1:c.527T>G	ENSP00000509686.1:p.Leu176Ter
ENST00000691903.1:c.527T>G	ENSP00000510314.1:p.Leu176Ter
ENST00000692776.1:c.527T>G	ENSP00000508524.1:p.Leu176Ter
ENST00000369452.9:c.527T>G MANE Select	ENSP00000358464.5:p.Leu176Ter
ENST00000265277.9:c.527T>G	ENSP00000265277.5:p.Leu176Ter
ENST00000369452.8:c.527T>G	ENSP00000358464.4:p.Leu176Ter
ENST00000451838.1:c.35T>G	ENSP00000408275.1:p.Leu12Ter
ENST00000489390.1:n.56-35530T>G
NM_001269039.1:c.527T>G	NP_001255968.1:p.Leu176Ter
NM_007373.3:c.527T>G , LRG_753t1:c.527T>G	NP_031399.2:p.Leu176Ter
XM_011540216.1:c.-380-20743T>G	XP_011538518.1:n.-380-20743T>G
NM_001269039.2:c.527T>G	NP_001255968.1:p.Leu176Ter
NM_001324336.1:c.527T>G	NP_001311265.1:p.Leu176Ter
NM_001324337.1:c.527T>G	NP_001311266.1:p.Leu176Ter
NR_136749.1:n.116-20743T>G
NM_007373.4:c.527T>G MANE Select	NP_031399.2:p.Leu176Ter
NM_001269039.3:c.527T>G	NP_001255968.1:p.Leu176Ter
NM_001324336.2:c.527T>G	NP_001311265.1:p.Leu176Ter
NM_001324337.2:c.527T>G	NP_001311266.1:p.Leu176Ter
NR_136749.2:n.55-20743T>G