Canonical Allele Identifier: CA387513204
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23333884T>C , CM000675.2:g.23333884T>C GRCh38
NC_000013.10:g.23908023T>C , CM000675.1:g.23908023T>C GRCh37
NC_000013.9:g.22806023T>C NCBI36
NG_012342.1:g.104819A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2185+19901A>G ENSP00000508399.1:n.2185+19901A>G
ENST00000682944.1:c.10019A>G ENSP00000507173.1:p.Gln3340Arg
ENST00000683210.1:c.2185+19901A>G ENSP00000506739.1:n.2185+19901A>G
ENST00000683270.1:c.6445+3538A>G ENSP00000507624.1:n.6445+3538A>G
ENST00000683367.1:c.2177-4400A>G ENSP00000507780.1:n.2177-4400A>G
ENST00000683489.1:c.2292-3932A>G ENSP00000508403.1:n.2292-3932A>G
ENST00000683680.1:c.2319-3932A>G ENSP00000507223.1:n.2319-3932A>G
ENST00000684163.1:c.2204-4400A>G ENSP00000508262.1:n.2204-4400A>G
ENST00000684196.1:n.4543-4400A>G
ENST00000684325.1:c.2186-12210A>G ENSP00000508121.1:n.2186-12210A>G
ENST00000684385.1:c.2221-4400A>G ENSP00000507855.1:n.2221-4400A>G
ENST00000684497.1:c.2186-11240A>G ENSP00000507057.1:n.2186-11240A>G
ENST00000382292.9:c.9992A>G MANE Select ENSP00000371729.3:p.Gln3331Arg
ENST00000423156.2:c.2186-4400A>G ENSP00000390925.2:n.2186-4400A>G
ENST00000455470.6:c.2432-4400A>G ENSP00000406565.2:n.2432-4400A>G
ENST00000382292.7:c.9992A>G ENSP00000371729.3:p.Gln3331Arg
ENST00000382298.7:c.9992A>G ENSP00000371735.3:p.Gln3331Arg
ENST00000402364.1:c.7742A>G ENSP00000385844.1:p.Gln2581Arg
ENST00000423156.1:c.1058-4400A>G ENSP00000390925.1:n.1058-4400A>G
ENST00000455470.5:c.2130-4400A>G
NM_001278055.1:c.9551A>G NP_001264984.1:p.Gln3184Arg
NM_014363.5:c.9992A>G NP_055178.3:p.Gln3331Arg
XM_005266338.1:c.10019A>G XP_005266395.1:p.Gln3340Arg
XM_011535038.1:c.10043A>G XP_011533340.1:p.Gln3348Arg
XM_011535039.1:c.10010A>G XP_011533341.1:p.Gln3337Arg
XM_005266338.2:c.10019A>G XP_005266395.1:p.Gln3340Arg
XM_011535039.2:c.10010A>G XP_011533341.1:p.Gln3337Arg
XM_017020539.1:c.9983A>G XP_016876028.1:p.Gln3328Arg
XM_024449337.1:c.10019A>G XP_024305105.1:p.Gln3340Arg
NM_014363.6:c.9992A>G MANE Select NP_055178.3:p.Gln3331Arg
NM_001278055.2:c.9551A>G NP_001264984.1:p.Gln3184Arg