Canonical Allele Identifier: CA2078631894
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23332737G= , CM000675.2:g.23332737G= GRCh38
NC_000013.10:g.23906876G= , CM000675.1:g.23906876G= GRCh37
NC_000013.9:g.22804876G= NCBI36
NG_012342.1:g.105966C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2186-20622C= ENSP00000508399.1:n.2186-20622C=
ENST00000682944.1:c.11166C= ENSP00000507173.1:p.Pro3722=
ENST00000683210.1:c.2185+21048C= ENSP00000506739.1:n.2185+21048C=
ENST00000683270.1:c.6446-3253C= ENSP00000507624.1:n.6446-3253C=
ENST00000683367.1:c.2177-3253C= ENSP00000507780.1:n.2177-3253C=
ENST00000683489.1:c.2292-2785C= ENSP00000508403.1:n.2292-2785C=
ENST00000683680.1:c.2319-2785C= ENSP00000507223.1:n.2319-2785C=
ENST00000684163.1:c.2204-3253C= ENSP00000508262.1:n.2204-3253C=
ENST00000684196.1:n.4543-3253C=
ENST00000684325.1:c.2186-11063C= ENSP00000508121.1:n.2186-11063C=
ENST00000684385.1:c.2221-3253C= ENSP00000507855.1:n.2221-3253C=
ENST00000684497.1:c.2186-10093C= ENSP00000507057.1:n.2186-10093C=
ENST00000382292.9:c.11139C= MANE Select ENSP00000371729.3:p.Pro3713=
ENST00000423156.2:c.2186-3253C= ENSP00000390925.2:n.2186-3253C=
ENST00000455470.6:c.2432-3253C= ENSP00000406565.2:n.2432-3253C=
ENST00000382292.7:c.11139C= ENSP00000371729.3:p.Pro3713=
ENST00000382298.7:c.11139C= ENSP00000371735.3:p.Pro3713=
ENST00000402364.1:c.8889C= ENSP00000385844.1:p.Pro2963=
ENST00000423156.1:c.1058-3253C= ENSP00000390925.1:n.1058-3253C=
ENST00000455470.5:c.2130-3253C=
NM_001278055.1:c.10698C= NP_001264984.1:p.Pro3566=
NM_014363.5:c.11139C= NP_055178.3:p.Pro3713=
XM_005266338.1:c.11166C= XP_005266395.1:p.Pro3722=
XM_011535038.1:c.11190C= XP_011533340.1:p.Pro3730=
XM_011535039.1:c.11157C= XP_011533341.1:p.Pro3719=
XM_005266338.2:c.11166C= XP_005266395.1:p.Pro3722=
XM_011535039.2:c.11157C= XP_011533341.1:p.Pro3719=
XM_017020539.1:c.11130C= XP_016876028.1:p.Pro3710=
XM_024449337.1:c.11166C= XP_024305105.1:p.Pro3722=
NM_014363.6:c.11139C= MANE Select NP_055178.3:p.Pro3713=
NM_001278055.2:c.10698C= NP_001264984.1:p.Pro3566=