Canonical Allele Identifier: CA2078644907

Gene: SACS

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23341642C= , CM000675.2:g.23341642C=	GRCh38
NC_000013.10:g.23915781C= , CM000675.1:g.23915781C=	GRCh37
NC_000013.9:g.22813781C=	NCBI36
NG_012342.1:g.97061G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+12143G=	ENSP00000508399.1:n.2185+12143G=
ENST00000682944.1:c.2261G=	ENSP00000507173.1:p.Arg754=
ENST00000683210.1:c.2185+12143G=	ENSP00000506739.1:n.2185+12143G=
ENST00000683270.1:c.2225G=	ENSP00000507624.1:p.Arg742=
ENST00000683367.1:c.2176+12143G=	ENSP00000507780.1:n.2176+12143G=
ENST00000683489.1:c.2234G=	ENSP00000508403.1:p.Arg745=
ENST00000683680.1:c.2261G=	ENSP00000507223.1:p.Arg754=
ENST00000684163.1:c.2203+5169G=	ENSP00000508262.1:n.2203+5169G=
ENST00000684196.1:n.4542+12143G=
ENST00000684325.1:c.2185+12143G=	ENSP00000508121.1:n.2185+12143G=
ENST00000684385.1:c.2220+5169G=	ENSP00000507855.1:n.2220+5169G=
ENST00000684497.1:c.2185+12143G=	ENSP00000507057.1:n.2185+12143G=
ENST00000382292.9:c.2234G= MANE Select	ENSP00000371729.3:p.Arg745=
ENST00000423156.2:c.2185+12143G=	ENSP00000390925.2:n.2185+12143G=
ENST00000455470.6:c.2234G=	ENSP00000406565.2:p.Arg745=
ENST00000382292.7:c.2234G=	ENSP00000371729.3:p.Arg745=
ENST00000382298.7:c.2234G=	ENSP00000371735.3:p.Arg745=
ENST00000402364.1:c.-17G=	ENSP00000385844.1:n.-17G=
ENST00000423156.1:c.1057+12143G=	ENSP00000390925.1:n.1057+12143G=
ENST00000455470.5:c.1932G=
NM_001278055.1:c.1793G=	NP_001264984.1:p.Arg598=
NM_014363.5:c.2234G=	NP_055178.3:p.Arg745=
XM_005266338.1:c.2261G=	XP_005266395.1:p.Arg754=
XM_011535038.1:c.2285G=	XP_011533340.1:p.Arg762=
XM_011535039.1:c.2252G=	XP_011533341.1:p.Arg751=
XM_005266338.2:c.2261G=	XP_005266395.1:p.Arg754=
XM_011535039.2:c.2252G=	XP_011533341.1:p.Arg751=
XM_017020539.1:c.2225G=	XP_016876028.1:p.Arg742=
XM_024449337.1:c.2261G=	XP_024305105.1:p.Arg754=
NM_014363.6:c.2234G= MANE Select	NP_055178.3:p.Arg745=
NM_001278055.2:c.1793G=	NP_001264984.1:p.Arg598=