Canonical Allele Identifier: CA2798500213

Gene: SACS

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23333874del , CM000675.2:g.23333874del	GRCh38
NC_000013.10:g.23908013del , CM000675.1:g.23908013del	GRCh37
NC_000013.9:g.22806013del	NCBI36
NG_012342.1:g.104829del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+19911del	ENSP00000508399.1:n.2185+19911del
ENST00000682944.1:c.10029del	ENSP00000507173.1:p.Asn3344ThrfsTer21
ENST00000683210.1:c.2185+19911del	ENSP00000506739.1:n.2185+19911del
ENST00000683270.1:c.6445+3548del	ENSP00000507624.1:n.6445+3548del
ENST00000683367.1:c.2177-4390del	ENSP00000507780.1:n.2177-4390del
ENST00000683489.1:c.2292-3922del	ENSP00000508403.1:n.2292-3922del
ENST00000683680.1:c.2319-3922del	ENSP00000507223.1:n.2319-3922del
ENST00000684163.1:c.2204-4390del	ENSP00000508262.1:n.2204-4390del
ENST00000684196.1:n.4543-4390del
ENST00000684325.1:c.2186-12200del	ENSP00000508121.1:n.2186-12200del
ENST00000684385.1:c.2221-4390del	ENSP00000507855.1:n.2221-4390del
ENST00000684497.1:c.2186-11230del	ENSP00000507057.1:n.2186-11230del
ENST00000382292.9:c.10002del MANE Select	ENSP00000371729.3:p.Asn3335ThrfsTer21
ENST00000423156.2:c.2186-4390del	ENSP00000390925.2:n.2186-4390del
ENST00000455470.6:c.2432-4390del	ENSP00000406565.2:n.2432-4390del
ENST00000382292.7:c.10002del	ENSP00000371729.3:p.Asn3335ThrfsTer21
ENST00000382298.7:c.10002del	ENSP00000371735.3:p.Asn3335ThrfsTer21
ENST00000402364.1:c.7752del	ENSP00000385844.1:p.Asn2585ThrfsTer21
ENST00000423156.1:c.1058-4390del	ENSP00000390925.1:n.1058-4390del
ENST00000455470.5:c.2130-4390del
NM_001278055.1:c.9561del	NP_001264984.1:p.Asn3188ThrfsTer21
NM_014363.5:c.10002del	NP_055178.3:p.Asn3335ThrfsTer21
XM_005266338.1:c.10029del	XP_005266395.1:p.Asn3344ThrfsTer21
XM_011535038.1:c.10053del	XP_011533340.1:p.Asn3352ThrfsTer21
XM_011535039.1:c.10020del	XP_011533341.1:p.Asn3341ThrfsTer21
XM_005266338.2:c.10029del	XP_005266395.1:p.Asn3344ThrfsTer21
XM_011535039.2:c.10020del	XP_011533341.1:p.Asn3341ThrfsTer21
XM_017020539.1:c.9993del	XP_016876028.1:p.Asn3332ThrfsTer21
XM_024449337.1:c.10029del	XP_024305105.1:p.Asn3344ThrfsTer21
NM_014363.6:c.10002del MANE Select	NP_055178.3:p.Asn3335ThrfsTer21
NM_001278055.2:c.9561del	NP_001264984.1:p.Asn3188ThrfsTer21