Canonical Allele Identifier: CA387542811

Gene: SACS

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23353794G>A , CM000675.2:g.23353794G>A	GRCh38
NC_000013.10:g.23927933G>A , CM000675.1:g.23927933G>A	GRCh37
NC_000013.9:g.22825933G>A	NCBI36
NG_012342.1:g.84909C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014363.6:c.2176C>T MANE Select	NP_055178.3:p.Gln726Ter
ENST00000382292.9:c.2176C>T MANE Select	ENSP00000371729.3:p.Gln726Ter
NM_001278055.1:c.1735C>T	NP_001264984.1:p.Gln579Ter
NM_001278055.2:c.1735C>T	NP_001264984.1:p.Gln579Ter
NM_014363.5:c.2176C>T	NP_055178.3:p.Gln726Ter
ENST00000382292.7:c.2176C>T	ENSP00000371729.3:p.Gln726Ter
ENST00000382298.7:c.2176C>T	ENSP00000371735.3:p.Gln726Ter
ENST00000402364.1:c.-75C>T	ENSP00000385844.1:n.-75C>T
ENST00000423156.1:c.1048C>T	ENSP00000390925.1:p.Gln350Ter
ENST00000423156.2:c.2176C>T	ENSP00000390925.2:p.Gln726Ter
ENST00000455470.5:c.1874C>T
ENST00000455470.6:c.2176C>T	ENSP00000406565.2:p.Gln726Ter
ENST00000476776.1:n.455C>T
ENST00000682775.1:c.2176C>T	ENSP00000508399.1:p.Gln726Ter
ENST00000682944.1:c.2176C>T	ENSP00000507173.1:p.Gln726Ter
ENST00000683210.1:c.2176C>T	ENSP00000506739.1:p.Gln726Ter
ENST00000683270.1:c.2167C>T	ENSP00000507624.1:p.Gln723Ter
ENST00000683367.1:c.2167C>T	ENSP00000507780.1:p.Gln723Ter
ENST00000683489.1:c.2176C>T	ENSP00000508403.1:p.Gln726Ter
ENST00000683680.1:c.2176C>T	ENSP00000507223.1:p.Gln726Ter
ENST00000684163.1:c.2167C>T	ENSP00000508262.1:p.Gln723Ter
ENST00000684196.1:n.4533C>T
ENST00000684325.1:c.2176C>T	ENSP00000508121.1:p.Gln726Ter
ENST00000684385.1:c.2176C>T	ENSP00000507855.1:p.Gln726Ter
ENST00000684497.1:c.2176C>T	ENSP00000507057.1:p.Gln726Ter
XM_005266338.1:c.2176C>T	XP_005266395.1:p.Gln726Ter
XM_005266338.2:c.2176C>T	XP_005266395.1:p.Gln726Ter
XM_011535038.1:c.2200C>T	XP_011533340.1:p.Gln734Ter
XM_011535039.1:c.2167C>T	XP_011533341.1:p.Gln723Ter
XM_011535039.2:c.2167C>T	XP_011533341.1:p.Gln723Ter
XM_017020539.1:c.2167C>T	XP_016876028.1:p.Gln723Ter
XM_024449337.1:c.2176C>T	XP_024305105.1:p.Gln726Ter