Canonical Allele Identifier: CA471507757

Gene: SHOC2

Linked Data

• gnomAD v4: 10-110964538-C-A
• MyVariant Identifiers: chr10:g.112724296C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110964538C>A , CM000672.2:g.110964538C>A	GRCh38
NC_000010.10:g.112724296C>A , CM000672.1:g.112724296C>A	GRCh37
NC_000010.9:g.112714286C>A	NCBI36
NG_028922.1:g.49996C>A , LRG_753:g.49996C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265277.10:c.180C>A	ENSP00000265277.5:p.Ala60=
ENST00000451838.2:c.-242-35877C>A	ENSP00000408275.2:n.-242-35877C>A
ENST00000480155.2:n.416C>A
ENST00000685059.1:c.180C>A	ENSP00000510210.1:p.Ala60=
ENST00000685613.1:c.180C>A	ENSP00000510564.1:p.Ala60=
ENST00000687592.1:n.479C>A
ENST00000688928.1:c.180C>A	ENSP00000509273.1:p.Ala60=
ENST00000689118.1:c.180C>A	ENSP00000510554.1:p.Ala60=
ENST00000689300.1:c.180C>A	ENSP00000510639.1:p.Ala60=
ENST00000689997.1:c.-380-21090C>A	ENSP00000510700.1:n.-380-21090C>A
ENST00000691151.1:n.472C>A
ENST00000691369.1:c.180C>A	ENSP00000509754.1:p.Ala60=
ENST00000691441.1:c.180C>A	ENSP00000509686.1:p.Ala60=
ENST00000691903.1:c.180C>A	ENSP00000510314.1:p.Ala60=
ENST00000692776.1:c.180C>A	ENSP00000508524.1:p.Ala60=
ENST00000369452.9:c.180C>A MANE Select	ENSP00000358464.5:p.Ala60=
ENST00000265277.9:c.180C>A	ENSP00000265277.5:p.Ala60=
ENST00000369452.8:c.180C>A	ENSP00000358464.4:p.Ala60=
ENST00000489390.1:n.56-35877C>A
ENST00000489783.1:n.558C>A
NM_001269039.1:c.180C>A	NP_001255968.1:p.Ala60=
NM_007373.3:c.180C>A , LRG_753t1:c.180C>A	NP_031399.2:p.Ala60=
XM_011540216.1:c.-380-21090C>A	XP_011538518.1:n.-380-21090C>A
NM_001269039.2:c.180C>A	NP_001255968.1:p.Ala60=
NM_001324336.1:c.180C>A	NP_001311265.1:p.Ala60=
NM_001324337.1:c.180C>A	NP_001311266.1:p.Ala60=
NR_136749.1:n.116-21090C>A
NM_007373.4:c.180C>A MANE Select	NP_031399.2:p.Ala60=
NM_001269039.3:c.180C>A	NP_001255968.1:p.Ala60=
NM_001324336.2:c.180C>A	NP_001311265.1:p.Ala60=
NM_001324337.2:c.180C>A	NP_001311266.1:p.Ala60=
NR_136749.2:n.55-21090C>A