Canonical Allele Identifier: CA2078636694

Gene: SACS

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23358587_23358590delinsAGAG , CM000675.2:g.23358587_23358590delinsAGAG	GRCh38
NC_000013.10:g.23932726_23932729delinsAGAG , CM000675.1:g.23932726_23932729delinsAGAG	GRCh37
NC_000013.9:g.22830726_22830729delinsAGAG	NCBI36
NG_012342.1:g.80113_80116delinsCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.458-109_458-106delinsCTCT	ENSP00000508399.1:n.458-109_458-106delinsCTCT
ENST00000682944.1:c.458-109_458-106delinsCTCT	ENSP00000507173.1:n.458-109_458-106delinsCTCT
ENST00000683154.1:n.596-109_596-106delinsCTCT
ENST00000683210.1:c.458-109_458-106delinsCTCT	ENSP00000506739.1:n.458-109_458-106delinsCTCT
ENST00000683270.1:c.449-109_449-106delinsCTCT	ENSP00000507624.1:n.449-109_449-106delinsCTCT
ENST00000683367.1:c.449-109_449-106delinsCTCT	ENSP00000507780.1:n.449-109_449-106delinsCTCT
ENST00000683489.1:c.458-109_458-106delinsCTCT	ENSP00000508403.1:n.458-109_458-106delinsCTCT
ENST00000683680.1:c.458-109_458-106delinsCTCT	ENSP00000507223.1:n.458-109_458-106delinsCTCT
ENST00000684163.1:c.449-109_449-106delinsCTCT	ENSP00000508262.1:n.449-109_449-106delinsCTCT
ENST00000684196.1:n.2815-109_2815-106delinsCTCT
ENST00000684325.1:c.458-109_458-106delinsCTCT	ENSP00000508121.1:n.458-109_458-106delinsCTCT
ENST00000684385.1:c.458-109_458-106delinsCTCT	ENSP00000507855.1:n.458-109_458-106delinsCTCT
ENST00000684497.1:c.458-109_458-106delinsCTCT	ENSP00000507057.1:n.458-109_458-106delinsCTCT
ENST00000382292.9:c.458-109_458-106delinsCTCT MANE Select	ENSP00000371729.3:n.458-109_458-106delinsCTCT
ENST00000423156.2:c.458-109_458-106delinsCTCT	ENSP00000390925.2:n.458-109_458-106delinsCTCT
ENST00000455470.6:c.458-109_458-106delinsCTCT	ENSP00000406565.2:n.458-109_458-106delinsCTCT
ENST00000382292.7:c.458-109_458-106delinsCTCT	ENSP00000371729.3:n.458-109_458-106delinsCTCT
ENST00000382298.7:c.458-109_458-106delinsCTCT	ENSP00000371735.3:n.458-109_458-106delinsCTCT
ENST00000402364.1:c.-1793-109_-1793-106delinsCTCT	ENSP00000385844.1:n.-1793-109_-1793-106delinsCTCT
ENST00000455470.5:c.156-109_156-106delinsCTCT
NM_001278055.1:c.17-109_17-106delinsCTCT	NP_001264984.1:n.17-109_17-106delinsCTCT
NM_014363.5:c.458-109_458-106delinsCTCT	NP_055178.3:n.458-109_458-106delinsCTCT
XM_005266338.1:c.458-109_458-106delinsCTCT	XP_005266395.1:n.458-109_458-106delinsCTCT
XM_011535038.1:c.482-109_482-106delinsCTCT	XP_011533340.1:n.482-109_482-106delinsCTCT
XM_011535039.1:c.449-109_449-106delinsCTCT	XP_011533341.1:n.449-109_449-106delinsCTCT
XM_005266338.2:c.458-109_458-106delinsCTCT	XP_005266395.1:n.458-109_458-106delinsCTCT
XM_011535039.2:c.449-109_449-106delinsCTCT	XP_011533341.1:n.449-109_449-106delinsCTCT
XM_017020539.1:c.449-109_449-106delinsCTCT	XP_016876028.1:n.449-109_449-106delinsCTCT
XM_024449337.1:c.458-109_458-106delinsCTCT	XP_024305105.1:n.458-109_458-106delinsCTCT
NM_014363.6:c.458-109_458-106delinsCTCT MANE Select	NP_055178.3:n.458-109_458-106delinsCTCT
NM_001278055.2:c.17-109_17-106delinsCTCT	NP_001264984.1:n.17-109_17-106delinsCTCT