Canonical Allele Identifier: CA2078656728

Gene: SACS

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23375171G= , CM000675.2:g.23375171G=	GRCh38
NC_000013.10:g.23949310G= , CM000675.1:g.23949310G=	GRCh37
NC_000013.9:g.22847310G=	NCBI36
NG_012342.1:g.63532C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682244.1:n.692C=
ENST00000682547.1:c.156C=	ENSP00000507735.1:p.Arg52=
ENST00000682775.1:c.119C=	ENSP00000508399.1:p.Ala40=
ENST00000682944.1:c.119C=	ENSP00000507173.1:p.Ala40=
ENST00000683154.1:n.257C=
ENST00000683210.1:c.119C=	ENSP00000506739.1:p.Ala40=
ENST00000683270.1:c.110C=	ENSP00000507624.1:p.Ala37=
ENST00000683367.1:c.110C=	ENSP00000507780.1:p.Ala37=
ENST00000683489.1:c.119C=	ENSP00000508403.1:p.Ala40=
ENST00000683680.1:c.119C=	ENSP00000507223.1:p.Ala40=
ENST00000684053.1:n.236C=
ENST00000684163.1:c.110C=	ENSP00000508262.1:p.Ala37=
ENST00000684325.1:c.119C=	ENSP00000508121.1:p.Ala40=
ENST00000684385.1:c.119C=	ENSP00000507855.1:p.Ala40=
ENST00000684497.1:c.119C=	ENSP00000507057.1:p.Ala40=
ENST00000382292.9:c.119C= MANE Select	ENSP00000371729.3:p.Ala40=
ENST00000423156.2:c.119C=	ENSP00000390925.2:p.Ala40=
ENST00000455470.6:c.119C=	ENSP00000406565.2:p.Ala40=
ENST00000382292.7:c.119C=	ENSP00000371729.3:p.Ala40=
ENST00000382298.7:c.119C=	ENSP00000371735.3:p.Ala40=
ENST00000402364.1:c.-2044C=	ENSP00000385844.1:n.-2044C=
NM_001278055.1:c.-235C=	NP_001264984.1:n.-235C=
NM_014363.5:c.119C=	NP_055178.3:p.Ala40=
XM_005266338.1:c.119C=	XP_005266395.1:p.Ala40=
XM_011535038.1:c.143C=	XP_011533340.1:p.Ala48=
XM_011535039.1:c.110C=	XP_011533341.1:p.Ala37=
XM_005266338.2:c.119C=	XP_005266395.1:p.Ala40=
XM_011535039.2:c.110C=	XP_011533341.1:p.Ala37=
XM_017020539.1:c.110C=	XP_016876028.1:p.Ala37=
XM_024449337.1:c.119C=	XP_024305105.1:p.Ala40=
NM_014363.6:c.119C= MANE Select	NP_055178.3:p.Ala40=
NM_001278055.2:c.-235C=	NP_001264984.1:n.-235C=