Canonical Allele Identifier: CA482928789
Gene: SACS HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.23949294C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23375155C>A , CM000675.2:g.23375155C>A GRCh38
NC_000013.10:g.23949294C>A , CM000675.1:g.23949294C>A GRCh37
NC_000013.9:g.22847294C>A NCBI36
NG_012342.1:g.63548G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682244.1:n.708G>T
ENST00000682547.1:c.172G>T ENSP00000507735.1:p.Gly58Cys
ENST00000682775.1:c.135G>T ENSP00000508399.1:p.Pro45=
ENST00000682944.1:c.135G>T ENSP00000507173.1:p.Pro45=
ENST00000683154.1:n.273G>T
ENST00000683210.1:c.135G>T ENSP00000506739.1:p.Pro45=
ENST00000683270.1:c.126G>T ENSP00000507624.1:p.Pro42=
ENST00000683367.1:c.126G>T ENSP00000507780.1:p.Pro42=
ENST00000683489.1:c.135G>T ENSP00000508403.1:p.Pro45=
ENST00000683680.1:c.135G>T ENSP00000507223.1:p.Pro45=
ENST00000684053.1:n.252G>T
ENST00000684163.1:c.126G>T ENSP00000508262.1:p.Pro42=
ENST00000684325.1:c.135G>T ENSP00000508121.1:p.Pro45=
ENST00000684385.1:c.135G>T ENSP00000507855.1:p.Pro45=
ENST00000684497.1:c.135G>T ENSP00000507057.1:p.Pro45=
ENST00000382292.9:c.135G>T MANE Select ENSP00000371729.3:p.Pro45=
ENST00000423156.2:c.135G>T ENSP00000390925.2:p.Pro45=
ENST00000455470.6:c.135G>T ENSP00000406565.2:p.Pro45=
ENST00000382292.7:c.135G>T ENSP00000371729.3:p.Pro45=
ENST00000382298.7:c.135G>T ENSP00000371735.3:p.Pro45=
ENST00000402364.1:c.-2028G>T ENSP00000385844.1:n.-2028G>T
NM_001278055.1:c.-219G>T NP_001264984.1:n.-219G>T
NM_014363.5:c.135G>T NP_055178.3:p.Pro45=
XM_005266338.1:c.135G>T XP_005266395.1:p.Pro45=
XM_011535038.1:c.159G>T XP_011533340.1:p.Pro53=
XM_011535039.1:c.126G>T XP_011533341.1:p.Pro42=
XM_005266338.2:c.135G>T XP_005266395.1:p.Pro45=
XM_011535039.2:c.126G>T XP_011533341.1:p.Pro42=
XM_017020539.1:c.126G>T XP_016876028.1:p.Pro42=
XM_024449337.1:c.135G>T XP_024305105.1:p.Pro45=
NM_014363.6:c.135G>T MANE Select NP_055178.3:p.Pro45=
NM_001278055.2:c.-219G>T NP_001264984.1:n.-219G>T