Canonical Allele Identifier: CA2078621291
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23334471T= , CM000675.2:g.23334471T= GRCh38
NC_000013.10:g.23908610T= , CM000675.1:g.23908610T= GRCh37
NC_000013.9:g.22806610T= NCBI36
NG_012342.1:g.104232A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+19314A= ENSP00000508399.1:n.2185+19314A=
ENST00000682944.1:c.9432A= ENSP00000507173.1:p.Leu3144=
ENST00000683210.1:c.2185+19314A= ENSP00000506739.1:n.2185+19314A=
ENST00000683270.1:c.6445+2951A= ENSP00000507624.1:n.6445+2951A=
ENST00000683367.1:c.2177-4987A= ENSP00000507780.1:n.2177-4987A=
ENST00000683489.1:c.2292-4519A= ENSP00000508403.1:n.2292-4519A=
ENST00000683680.1:c.2319-4519A= ENSP00000507223.1:n.2319-4519A=
ENST00000684163.1:c.2204-4987A= ENSP00000508262.1:n.2204-4987A=
ENST00000684196.1:n.4543-4987A=
ENST00000684325.1:c.2186-12797A= ENSP00000508121.1:n.2186-12797A=
ENST00000684385.1:c.2221-4987A= ENSP00000507855.1:n.2221-4987A=
ENST00000684497.1:c.2186-11827A= ENSP00000507057.1:n.2186-11827A=
ENST00000382292.9:c.9405A= MANE Select ENSP00000371729.3:p.Leu3135=
ENST00000423156.2:c.2186-4987A= ENSP00000390925.2:n.2186-4987A=
ENST00000455470.6:c.2432-4987A= ENSP00000406565.2:n.2432-4987A=
ENST00000382292.7:c.9405A= ENSP00000371729.3:p.Leu3135=
ENST00000382298.7:c.9405A= ENSP00000371735.3:p.Leu3135=
ENST00000402364.1:c.7155A= ENSP00000385844.1:p.Leu2385=
ENST00000423156.1:c.1058-4987A= ENSP00000390925.1:n.1058-4987A=
ENST00000455470.5:c.2130-4987A=
NM_001278055.1:c.8964A= NP_001264984.1:p.Leu2988=
NM_014363.5:c.9405A= NP_055178.3:p.Leu3135=
XM_005266338.1:c.9432A= XP_005266395.1:p.Leu3144=
XM_011535038.1:c.9456A= XP_011533340.1:p.Leu3152=
XM_011535039.1:c.9423A= XP_011533341.1:p.Leu3141=
XM_005266338.2:c.9432A= XP_005266395.1:p.Leu3144=
XM_011535039.2:c.9423A= XP_011533341.1:p.Leu3141=
XM_017020539.1:c.9396A= XP_016876028.1:p.Leu3132=
XM_024449337.1:c.9432A= XP_024305105.1:p.Leu3144=
NM_014363.6:c.9405A= MANE Select NP_055178.3:p.Leu3135=
NM_001278055.2:c.8964A= NP_001264984.1:p.Leu2988=