Canonical Allele Identifier: CA2529349850

Gene: SACS

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23358421_23358422insACATTCT , CM000675.2:g.23358421_23358422insACATTCT	GRCh38
NC_000013.10:g.23932560_23932561insACATTCT , CM000675.1:g.23932560_23932561insACATTCT	GRCh37
NC_000013.9:g.22830560_22830561insACATTCT	NCBI36
NG_012342.1:g.80282_80283insGAATGTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.518_519insGAATGTA	ENSP00000508399.1:p.Glu174AsnfsTer12
ENST00000682944.1:c.518_519insGAATGTA	ENSP00000507173.1:p.Glu174AsnfsTer12
ENST00000683154.1:n.656_657insGAATGTA
ENST00000683210.1:c.518_519insGAATGTA	ENSP00000506739.1:p.Glu174AsnfsTer12
ENST00000683270.1:c.509_510insGAATGTA	ENSP00000507624.1:p.Glu171AsnfsTer12
ENST00000683367.1:c.509_510insGAATGTA	ENSP00000507780.1:p.Glu171AsnfsTer12
ENST00000683489.1:c.518_519insGAATGTA	ENSP00000508403.1:p.Glu174AsnfsTer12
ENST00000683680.1:c.518_519insGAATGTA	ENSP00000507223.1:p.Glu174AsnfsTer12
ENST00000684163.1:c.509_510insGAATGTA	ENSP00000508262.1:p.Glu171AsnfsTer12
ENST00000684196.1:n.2875_2876insGAATGTA
ENST00000684325.1:c.518_519insGAATGTA	ENSP00000508121.1:p.Glu174AsnfsTer12
ENST00000684385.1:c.518_519insGAATGTA	ENSP00000507855.1:p.Glu174AsnfsTer12
ENST00000684497.1:c.518_519insGAATGTA	ENSP00000507057.1:p.Glu174AsnfsTer12
ENST00000382292.9:c.518_519insGAATGTA MANE Select	ENSP00000371729.3:p.Glu174AsnfsTer12
ENST00000423156.2:c.518_519insGAATGTA	ENSP00000390925.2:p.Glu174AsnfsTer12
ENST00000455470.6:c.518_519insGAATGTA	ENSP00000406565.2:p.Glu174AsnfsTer12
ENST00000382292.7:c.518_519insGAATGTA	ENSP00000371729.3:p.Glu174AsnfsTer12
ENST00000382298.7:c.518_519insGAATGTA	ENSP00000371735.3:p.Glu174AsnfsTer12
ENST00000402364.1:c.-1733_-1732insGAATGTA	ENSP00000385844.1:n.-1733_-1732insGAATGTA
ENST00000455470.5:c.216_217insGAATGTA
NM_001278055.1:c.77_78insGAATGTA	NP_001264984.1:p.Glu27AsnfsTer12
NM_014363.5:c.518_519insGAATGTA	NP_055178.3:p.Glu174AsnfsTer12
XM_005266338.1:c.518_519insGAATGTA	XP_005266395.1:p.Glu174AsnfsTer12
XM_011535038.1:c.542_543insGAATGTA	XP_011533340.1:p.Glu182AsnfsTer12
XM_011535039.1:c.509_510insGAATGTA	XP_011533341.1:p.Glu171AsnfsTer12
XM_005266338.2:c.518_519insGAATGTA	XP_005266395.1:p.Glu174AsnfsTer12
XM_011535039.2:c.509_510insGAATGTA	XP_011533341.1:p.Glu171AsnfsTer12
XM_017020539.1:c.509_510insGAATGTA	XP_016876028.1:p.Glu171AsnfsTer12
XM_024449337.1:c.518_519insGAATGTA	XP_024305105.1:p.Glu174AsnfsTer12
NM_014363.6:c.518_519insGAATGTA MANE Select	NP_055178.3:p.Glu174AsnfsTer12
NM_001278055.2:c.77_78insGAATGTA	NP_001264984.1:p.Glu27AsnfsTer12