Canonical Allele Identifier: CA387512181
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23333423T>A , CM000675.2:g.23333423T>A GRCh38
NC_000013.10:g.23907562T>A , CM000675.1:g.23907562T>A GRCh37
NC_000013.9:g.22805562T>A NCBI36
NG_012342.1:g.105280A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+20362A>T ENSP00000508399.1:n.2185+20362A>T
ENST00000682944.1:c.10480A>T ENSP00000507173.1:p.Ile3494Phe
ENST00000683210.1:c.2185+20362A>T ENSP00000506739.1:n.2185+20362A>T
ENST00000683270.1:c.6446-3939A>T ENSP00000507624.1:n.6446-3939A>T
ENST00000683367.1:c.2177-3939A>T ENSP00000507780.1:n.2177-3939A>T
ENST00000683489.1:c.2292-3471A>T ENSP00000508403.1:n.2292-3471A>T
ENST00000683680.1:c.2319-3471A>T ENSP00000507223.1:n.2319-3471A>T
ENST00000684163.1:c.2204-3939A>T ENSP00000508262.1:n.2204-3939A>T
ENST00000684196.1:n.4543-3939A>T
ENST00000684325.1:c.2186-11749A>T ENSP00000508121.1:n.2186-11749A>T
ENST00000684385.1:c.2221-3939A>T ENSP00000507855.1:n.2221-3939A>T
ENST00000684497.1:c.2186-10779A>T ENSP00000507057.1:n.2186-10779A>T
ENST00000382292.9:c.10453A>T MANE Select ENSP00000371729.3:p.Ile3485Phe
ENST00000423156.2:c.2186-3939A>T ENSP00000390925.2:n.2186-3939A>T
ENST00000455470.6:c.2432-3939A>T ENSP00000406565.2:n.2432-3939A>T
ENST00000382292.7:c.10453A>T ENSP00000371729.3:p.Ile3485Phe
ENST00000382298.7:c.10453A>T ENSP00000371735.3:p.Ile3485Phe
ENST00000402364.1:c.8203A>T ENSP00000385844.1:p.Ile2735Phe
ENST00000423156.1:c.1058-3939A>T ENSP00000390925.1:n.1058-3939A>T
ENST00000455470.5:c.2130-3939A>T
NM_001278055.1:c.10012A>T NP_001264984.1:p.Ile3338Phe
NM_014363.5:c.10453A>T NP_055178.3:p.Ile3485Phe
XM_005266338.1:c.10480A>T XP_005266395.1:p.Ile3494Phe
XM_011535038.1:c.10504A>T XP_011533340.1:p.Ile3502Phe
XM_011535039.1:c.10471A>T XP_011533341.1:p.Ile3491Phe
XM_005266338.2:c.10480A>T XP_005266395.1:p.Ile3494Phe
XM_011535039.2:c.10471A>T XP_011533341.1:p.Ile3491Phe
XM_017020539.1:c.10444A>T XP_016876028.1:p.Ile3482Phe
XM_024449337.1:c.10480A>T XP_024305105.1:p.Ile3494Phe
NM_014363.6:c.10453A>T MANE Select NP_055178.3:p.Ile3485Phe
NM_001278055.2:c.10012A>T NP_001264984.1:p.Ile3338Phe