Canonical Allele Identifier: CA5689679

Gene: SHOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.111000459C>T , CM000672.2:g.111000459C>T	GRCh38
NC_000010.10:g.112760217C>T , CM000672.1:g.112760217C>T	GRCh37
NC_000010.9:g.112750207C>T	NCBI36
NG_028922.1:g.85917C>T , LRG_753:g.85917C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265277.10:c.748C>T	ENSP00000265277.5:p.Leu250=
ENST00000451838.2:c.-198C>T	ENSP00000408275.2:n.-198C>T
ENST00000685059.1:c.886C>T	ENSP00000510210.1:p.Leu296=
ENST00000685613.1:c.842-4147C>T	ENSP00000510564.1:n.842-4147C>T
ENST00000687592.1:n.1185C>T
ENST00000688928.1:c.886C>T	ENSP00000509273.1:p.Leu296=
ENST00000689118.1:c.886C>T	ENSP00000510554.1:p.Leu296=
ENST00000689300.1:c.886C>T	ENSP00000510639.1:p.Leu296=
ENST00000689997.1:c.-198C>T	ENSP00000510700.1:n.-198C>T
ENST00000691369.1:c.886C>T	ENSP00000509754.1:p.Leu296=
ENST00000691441.1:c.886C>T	ENSP00000509686.1:p.Leu296=
ENST00000691903.1:c.886C>T	ENSP00000510314.1:p.Leu296=
ENST00000692776.1:c.886C>T	ENSP00000508524.1:p.Leu296=
ENST00000369452.9:c.886C>T MANE Select	ENSP00000358464.5:p.Leu296=
ENST00000265277.9:c.748C>T	ENSP00000265277.5:p.Leu250=
ENST00000369452.8:c.886C>T	ENSP00000358464.4:p.Leu296=
ENST00000451838.1:c.256C>T	ENSP00000408275.1:p.Leu86=
ENST00000489390.1:n.100C>T
NM_001269039.1:c.748C>T	NP_001255968.1:p.Leu250=
NM_007373.3:c.886C>T , LRG_753t1:c.886C>T	NP_031399.2:p.Leu296=
XM_011540216.1:c.-198C>T	XP_011538518.1:n.-198C>T
NM_001269039.2:c.748C>T	NP_001255968.1:p.Leu250=
NM_001324336.1:c.886C>T	NP_001311265.1:p.Leu296=
NM_001324337.1:c.886C>T	NP_001311266.1:p.Leu296=
NR_136749.1:n.298C>T
NM_007373.4:c.886C>T MANE Select	NP_031399.2:p.Leu296=
NM_001269039.3:c.748C>T	NP_001255968.1:p.Leu250=
NM_001324336.2:c.886C>T	NP_001311265.1:p.Leu296=
NM_001324337.2:c.886C>T	NP_001311266.1:p.Leu296=
NR_136749.2:n.237C>T