Canonical Allele Identifier: CA2078622108
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23334876A= , CM000675.2:g.23334876A= GRCh38
NC_000013.10:g.23909015A= , CM000675.1:g.23909015A= GRCh37
NC_000013.9:g.22807015A= NCBI36
NG_012342.1:g.103827T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+18909T= ENSP00000508399.1:n.2185+18909T=
ENST00000682944.1:c.9027T= ENSP00000507173.1:p.Asn3009=
ENST00000683210.1:c.2185+18909T= ENSP00000506739.1:n.2185+18909T=
ENST00000683270.1:c.6445+2546T= ENSP00000507624.1:n.6445+2546T=
ENST00000683367.1:c.2177-5392T= ENSP00000507780.1:n.2177-5392T=
ENST00000683489.1:c.2292-4924T= ENSP00000508403.1:n.2292-4924T=
ENST00000683680.1:c.2319-4924T= ENSP00000507223.1:n.2319-4924T=
ENST00000684163.1:c.2204-5392T= ENSP00000508262.1:n.2204-5392T=
ENST00000684196.1:n.4543-5392T=
ENST00000684325.1:c.2186-13202T= ENSP00000508121.1:n.2186-13202T=
ENST00000684385.1:c.2221-5392T= ENSP00000507855.1:n.2221-5392T=
ENST00000684497.1:c.2186-12232T= ENSP00000507057.1:n.2186-12232T=
ENST00000382292.9:c.9000T= MANE Select ENSP00000371729.3:p.Asn3000=
ENST00000423156.2:c.2186-5392T= ENSP00000390925.2:n.2186-5392T=
ENST00000455470.6:c.2432-5392T= ENSP00000406565.2:n.2432-5392T=
ENST00000382292.7:c.9000T= ENSP00000371729.3:p.Asn3000=
ENST00000382298.7:c.9000T= ENSP00000371735.3:p.Asn3000=
ENST00000402364.1:c.6750T= ENSP00000385844.1:p.Asn2250=
ENST00000423156.1:c.1058-5392T= ENSP00000390925.1:n.1058-5392T=
ENST00000455470.5:c.2130-5392T=
NM_001278055.1:c.8559T= NP_001264984.1:p.Asn2853=
NM_014363.5:c.9000T= NP_055178.3:p.Asn3000=
XM_005266338.1:c.9027T= XP_005266395.1:p.Asn3009=
XM_011535038.1:c.9051T= XP_011533340.1:p.Asn3017=
XM_011535039.1:c.9018T= XP_011533341.1:p.Asn3006=
XM_005266338.2:c.9027T= XP_005266395.1:p.Asn3009=
XM_011535039.2:c.9018T= XP_011533341.1:p.Asn3006=
XM_017020539.1:c.8991T= XP_016876028.1:p.Asn2997=
XM_024449337.1:c.9027T= XP_024305105.1:p.Asn3009=
NM_014363.6:c.9000T= MANE Select NP_055178.3:p.Asn3000=
NM_001278055.2:c.8559T= NP_001264984.1:p.Asn2853=