Canonical Allele Identifier: CA2518850541
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23358417_23358418insAGAAAATATTATA , CM000675.2:g.23358417_23358418insAGAAAATATTATA GRCh38
NC_000013.10:g.23932556_23932557insAGAAAATATTATA , CM000675.1:g.23932556_23932557insAGAAAATATTATA GRCh37
NC_000013.9:g.22830556_22830557insAGAAAATATTATA NCBI36
NG_012342.1:g.80285_80286insTATAATATTTTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.521_522insTATAATATTTTCT ENSP00000508399.1:p.Glu174AspfsTer14
ENST00000682944.1:c.521_522insTATAATATTTTCT ENSP00000507173.1:p.Glu174AspfsTer14
ENST00000683154.1:n.659_660insTATAATATTTTCT
ENST00000683210.1:c.521_522insTATAATATTTTCT ENSP00000506739.1:p.Glu174AspfsTer14
ENST00000683270.1:c.512_513insTATAATATTTTCT ENSP00000507624.1:p.Glu171AspfsTer14
ENST00000683367.1:c.512_513insTATAATATTTTCT ENSP00000507780.1:p.Glu171AspfsTer14
ENST00000683489.1:c.521_522insTATAATATTTTCT ENSP00000508403.1:p.Glu174AspfsTer14
ENST00000683680.1:c.521_522insTATAATATTTTCT ENSP00000507223.1:p.Glu174AspfsTer14
ENST00000684163.1:c.512_513insTATAATATTTTCT ENSP00000508262.1:p.Glu171AspfsTer14
ENST00000684196.1:n.2878_2879insTATAATATTTTCT
ENST00000684325.1:c.521_522insTATAATATTTTCT ENSP00000508121.1:p.Glu174AspfsTer14
ENST00000684385.1:c.521_522insTATAATATTTTCT ENSP00000507855.1:p.Glu174AspfsTer14
ENST00000684497.1:c.521_522insTATAATATTTTCT ENSP00000507057.1:p.Glu174AspfsTer14
ENST00000382292.9:c.521_522insTATAATATTTTCT MANE Select ENSP00000371729.3:p.Glu174AspfsTer14
ENST00000423156.2:c.521_522insTATAATATTTTCT ENSP00000390925.2:p.Glu174AspfsTer14
ENST00000455470.6:c.521_522insTATAATATTTTCT ENSP00000406565.2:p.Glu174AspfsTer14
ENST00000382292.7:c.521_522insTATAATATTTTCT ENSP00000371729.3:p.Glu174AspfsTer14
ENST00000382298.7:c.521_522insTATAATATTTTCT ENSP00000371735.3:p.Glu174AspfsTer14
ENST00000402364.1:c.-1730_-1729insTATAATATTTTCT ENSP00000385844.1:n.-1730_-1729insTATAATATTTTCT
ENST00000455470.5:c.219_220insTATAATATTTTCT
NM_001278055.1:c.80_81insTATAATATTTTCT NP_001264984.1:p.Glu27AspfsTer14
NM_014363.5:c.521_522insTATAATATTTTCT NP_055178.3:p.Glu174AspfsTer14
XM_005266338.1:c.521_522insTATAATATTTTCT XP_005266395.1:p.Glu174AspfsTer14
XM_011535038.1:c.545_546insTATAATATTTTCT XP_011533340.1:p.Glu182AspfsTer14
XM_011535039.1:c.512_513insTATAATATTTTCT XP_011533341.1:p.Glu171AspfsTer14
XM_005266338.2:c.521_522insTATAATATTTTCT XP_005266395.1:p.Glu174AspfsTer14
XM_011535039.2:c.512_513insTATAATATTTTCT XP_011533341.1:p.Glu171AspfsTer14
XM_017020539.1:c.512_513insTATAATATTTTCT XP_016876028.1:p.Glu171AspfsTer14
XM_024449337.1:c.521_522insTATAATATTTTCT XP_024305105.1:p.Glu174AspfsTer14
NM_014363.6:c.521_522insTATAATATTTTCT MANE Select NP_055178.3:p.Glu174AspfsTer14
NM_001278055.2:c.80_81insTATAATATTTTCT NP_001264984.1:p.Glu27AspfsTer14