Canonical Allele Identifier: CA2831039796

Gene: SACS

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23355217_23355233delinsC , CM000675.2:g.23355217_23355233delinsC	GRCh38
NC_000013.10:g.23929356_23929372delinsC , CM000675.1:g.23929356_23929372delinsC	GRCh37
NC_000013.9:g.22827356_22827372delinsC	NCBI36
NG_012342.1:g.83470_83486delinsG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.1379_1395delinsG	ENSP00000508399.1:p.Leu460ArgfsTer13
ENST00000682944.1:c.1379_1395delinsG	ENSP00000507173.1:p.Leu460ArgfsTer13
ENST00000683154.1:n.1517_1533delinsG
ENST00000683210.1:c.1379_1395delinsG	ENSP00000506739.1:p.Leu460ArgfsTer13
ENST00000683270.1:c.1370_1386delinsG	ENSP00000507624.1:p.Leu457ArgfsTer13
ENST00000683367.1:c.1370_1386delinsG	ENSP00000507780.1:p.Leu457ArgfsTer13
ENST00000683489.1:c.1379_1395delinsG	ENSP00000508403.1:p.Leu460ArgfsTer13
ENST00000683680.1:c.1379_1395delinsG	ENSP00000507223.1:p.Leu460ArgfsTer13
ENST00000684163.1:c.1370_1386delinsG	ENSP00000508262.1:p.Leu457ArgfsTer13
ENST00000684196.1:n.3736_3752delinsG
ENST00000684325.1:c.1379_1395delinsG	ENSP00000508121.1:p.Leu460ArgfsTer13
ENST00000684385.1:c.1379_1395delinsG	ENSP00000507855.1:p.Leu460ArgfsTer13
ENST00000684497.1:c.1379_1395delinsG	ENSP00000507057.1:p.Leu460ArgfsTer13
ENST00000382292.9:c.1379_1395delinsG MANE Select	ENSP00000371729.3:p.Leu460ArgfsTer13
ENST00000423156.2:c.1379_1395delinsG	ENSP00000390925.2:p.Leu460ArgfsTer13
ENST00000455470.6:c.1379_1395delinsG	ENSP00000406565.2:p.Leu460ArgfsTer13
ENST00000382292.7:c.1379_1395delinsG	ENSP00000371729.3:p.Leu460ArgfsTer13
ENST00000382298.7:c.1379_1395delinsG	ENSP00000371735.3:p.Leu460ArgfsTer13
ENST00000402364.1:c.-872_-856delinsG	ENSP00000385844.1:n.-872_-856delinsG
ENST00000423156.1:c.251_267delinsG	ENSP00000390925.1:p.Leu84ArgfsTer13
ENST00000455470.5:c.1077_1093delinsG
NM_001278055.1:c.938_954delinsG	NP_001264984.1:p.Leu313ArgfsTer13
NM_014363.5:c.1379_1395delinsG	NP_055178.3:p.Leu460ArgfsTer13
XM_005266338.1:c.1379_1395delinsG	XP_005266395.1:p.Leu460ArgfsTer13
XM_011535038.1:c.1403_1419delinsG	XP_011533340.1:p.Leu468ArgfsTer13
XM_011535039.1:c.1370_1386delinsG	XP_011533341.1:p.Leu457ArgfsTer13
XM_005266338.2:c.1379_1395delinsG	XP_005266395.1:p.Leu460ArgfsTer13
XM_011535039.2:c.1370_1386delinsG	XP_011533341.1:p.Leu457ArgfsTer13
XM_017020539.1:c.1370_1386delinsG	XP_016876028.1:p.Leu457ArgfsTer13
XM_024449337.1:c.1379_1395delinsG	XP_024305105.1:p.Leu460ArgfsTer13
NM_014363.6:c.1379_1395delinsG MANE Select	NP_055178.3:p.Leu460ArgfsTer13
NM_001278055.2:c.938_954delinsG	NP_001264984.1:p.Leu313ArgfsTer13