Canonical Allele Identifier: CA2078629362
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23331190A= , CM000675.2:g.23331190A= GRCh38
NC_000013.10:g.23905329A= , CM000675.1:g.23905329A= GRCh37
NC_000013.9:g.22803329A= NCBI36
NG_012342.1:g.107513T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2186-19075T= ENSP00000508399.1:n.2186-19075T=
ENST00000682944.1:c.12713T= ENSP00000507173.1:p.Ile4238=
ENST00000683210.1:c.2185+22595T= ENSP00000506739.1:n.2185+22595T=
ENST00000683270.1:c.6446-1706T= ENSP00000507624.1:n.6446-1706T=
ENST00000683367.1:c.2177-1706T= ENSP00000507780.1:n.2177-1706T=
ENST00000683489.1:c.2292-1238T= ENSP00000508403.1:n.2292-1238T=
ENST00000683680.1:c.2319-1238T= ENSP00000507223.1:n.2319-1238T=
ENST00000684163.1:c.2204-1706T= ENSP00000508262.1:n.2204-1706T=
ENST00000684196.1:n.4543-1706T=
ENST00000684325.1:c.2186-9516T= ENSP00000508121.1:n.2186-9516T=
ENST00000684385.1:c.2221-1706T= ENSP00000507855.1:n.2221-1706T=
ENST00000684497.1:c.2186-8546T= ENSP00000507057.1:n.2186-8546T=
ENST00000382292.9:c.12686T= MANE Select ENSP00000371729.3:p.Ile4229=
ENST00000423156.2:c.2186-1706T= ENSP00000390925.2:n.2186-1706T=
ENST00000455470.6:c.2432-1706T= ENSP00000406565.2:n.2432-1706T=
ENST00000382292.7:c.12686T= ENSP00000371729.3:p.Ile4229=
ENST00000382298.7:c.12686T= ENSP00000371735.3:p.Ile4229=
ENST00000402364.1:c.10436T= ENSP00000385844.1:p.Ile3479=
ENST00000423156.1:c.1058-1706T= ENSP00000390925.1:n.1058-1706T=
ENST00000455470.5:c.2130-1706T=
NM_001278055.1:c.12245T= NP_001264984.1:p.Ile4082=
NM_014363.5:c.12686T= NP_055178.3:p.Ile4229=
XM_005266338.1:c.12713T= XP_005266395.1:p.Ile4238=
XM_011535038.1:c.12737T= XP_011533340.1:p.Ile4246=
XM_011535039.1:c.12704T= XP_011533341.1:p.Ile4235=
XM_005266338.2:c.12713T= XP_005266395.1:p.Ile4238=
XM_011535039.2:c.12704T= XP_011533341.1:p.Ile4235=
XM_017020539.1:c.12677T= XP_016876028.1:p.Ile4226=
XM_024449337.1:c.12713T= XP_024305105.1:p.Ile4238=
NM_014363.6:c.12686T= MANE Select NP_055178.3:p.Ile4229=
NM_001278055.2:c.12245T= NP_001264984.1:p.Ile4082=