Canonical Allele Identifier: CA2078623767
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23335597T= , CM000675.2:g.23335597T= GRCh38
NC_000013.10:g.23909736T= , CM000675.1:g.23909736T= GRCh37
NC_000013.9:g.22807736T= NCBI36
NG_012342.1:g.103106A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+18188A= ENSP00000508399.1:n.2185+18188A=
ENST00000682944.1:c.8306A= ENSP00000507173.1:p.Asn2769=
ENST00000683210.1:c.2185+18188A= ENSP00000506739.1:n.2185+18188A=
ENST00000683270.1:c.6445+1825A= ENSP00000507624.1:n.6445+1825A=
ENST00000683367.1:c.2177-6113A= ENSP00000507780.1:n.2177-6113A=
ENST00000683489.1:c.2292-5645A= ENSP00000508403.1:n.2292-5645A=
ENST00000683680.1:c.2319-5645A= ENSP00000507223.1:n.2319-5645A=
ENST00000684163.1:c.2204-6113A= ENSP00000508262.1:n.2204-6113A=
ENST00000684196.1:n.4543-6113A=
ENST00000684325.1:c.2186-13923A= ENSP00000508121.1:n.2186-13923A=
ENST00000684385.1:c.2221-6113A= ENSP00000507855.1:n.2221-6113A=
ENST00000684497.1:c.2186-12953A= ENSP00000507057.1:n.2186-12953A=
ENST00000382292.9:c.8279A= MANE Select ENSP00000371729.3:p.Asn2760=
ENST00000423156.2:c.2186-6113A= ENSP00000390925.2:n.2186-6113A=
ENST00000455470.6:c.2431+5848A= ENSP00000406565.2:n.2431+5848A=
ENST00000382292.7:c.8279A= ENSP00000371729.3:p.Asn2760=
ENST00000382298.7:c.8279A= ENSP00000371735.3:p.Asn2760=
ENST00000402364.1:c.6029A= ENSP00000385844.1:p.Asn2010=
ENST00000423156.1:c.1058-6113A= ENSP00000390925.1:n.1058-6113A=
ENST00000455470.5:c.2129+5848A=
NM_001278055.1:c.7838A= NP_001264984.1:p.Asn2613=
NM_014363.5:c.8279A= NP_055178.3:p.Asn2760=
XM_005266338.1:c.8306A= XP_005266395.1:p.Asn2769=
XM_011535038.1:c.8330A= XP_011533340.1:p.Asn2777=
XM_011535039.1:c.8297A= XP_011533341.1:p.Asn2766=
XM_005266338.2:c.8306A= XP_005266395.1:p.Asn2769=
XM_011535039.2:c.8297A= XP_011533341.1:p.Asn2766=
XM_017020539.1:c.8270A= XP_016876028.1:p.Asn2757=
XM_024449337.1:c.8306A= XP_024305105.1:p.Asn2769=
NM_014363.6:c.8279A= MANE Select NP_055178.3:p.Asn2760=
NM_001278055.2:c.7838A= NP_001264984.1:p.Asn2613=