Canonical Allele Identifier: CA6912089

Gene: SACS

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23365176C>T , CM000675.2:g.23365176C>T	GRCh38
NC_000013.10:g.23939315C>T , CM000675.1:g.23939315C>T	GRCh37
NC_000013.9:g.22837315C>T	NCBI36
NG_012342.1:g.73527G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014363.6:c.447G>A MANE Select	NP_055178.3:p.Ala149=
ENST00000382292.9:c.447G>A MANE Select	ENSP00000371729.3:p.Ala149=
NM_001278055.1:c.6G>A	NP_001264984.1:p.Ala2=
NM_001278055.2:c.6G>A	NP_001264984.1:p.Ala2=
NM_014363.5:c.447G>A	NP_055178.3:p.Ala149=
ENST00000382292.7:c.447G>A	ENSP00000371729.3:p.Ala149=
ENST00000382298.7:c.447G>A	ENSP00000371735.3:p.Ala149=
ENST00000402364.1:c.-1804G>A	ENSP00000385844.1:n.-1804G>A
ENST00000423156.2:c.447G>A	ENSP00000390925.2:p.Ala149=
ENST00000455470.5:c.145G>A
ENST00000455470.6:c.447G>A	ENSP00000406565.2:p.Ala149=
ENST00000682244.1:n.1020G>A
ENST00000682354.1:n.1212G>A
ENST00000682775.1:c.447G>A	ENSP00000508399.1:p.Ala149=
ENST00000682944.1:c.447G>A	ENSP00000507173.1:p.Ala149=
ENST00000683154.1:n.585G>A
ENST00000683210.1:c.447G>A	ENSP00000506739.1:p.Ala149=
ENST00000683270.1:c.438G>A	ENSP00000507624.1:p.Ala146=
ENST00000683367.1:c.438G>A	ENSP00000507780.1:p.Ala146=
ENST00000683489.1:c.447G>A	ENSP00000508403.1:p.Ala149=
ENST00000683680.1:c.447G>A	ENSP00000507223.1:p.Ala149=
ENST00000684053.1:n.564G>A
ENST00000684163.1:c.438G>A	ENSP00000508262.1:p.Ala146=
ENST00000684196.1:n.2804G>A
ENST00000684325.1:c.447G>A	ENSP00000508121.1:p.Ala149=
ENST00000684385.1:c.447G>A	ENSP00000507855.1:p.Ala149=
ENST00000684497.1:c.447G>A	ENSP00000507057.1:p.Ala149=
XM_005266338.1:c.447G>A	XP_005266395.1:p.Ala149=
XM_005266338.2:c.447G>A	XP_005266395.1:p.Ala149=
XM_011535038.1:c.471G>A	XP_011533340.1:p.Ala157=
XM_011535039.1:c.438G>A	XP_011533341.1:p.Ala146=
XM_011535039.2:c.438G>A	XP_011533341.1:p.Ala146=
XM_017020539.1:c.438G>A	XP_016876028.1:p.Ala146=
XM_024449337.1:c.447G>A	XP_024305105.1:p.Ala149=