Canonical Allele Identifier: CA387521498
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23337335C>T , CM000675.2:g.23337335C>T GRCh38
NC_000013.10:g.23911474C>T , CM000675.1:g.23911474C>T GRCh37
NC_000013.9:g.22809474C>T NCBI36
NG_012342.1:g.101368G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2185+16450G>A ENSP00000508399.1:n.2185+16450G>A
ENST00000682944.1:c.6568G>A ENSP00000507173.1:p.Ala2190Thr
ENST00000683210.1:c.2185+16450G>A ENSP00000506739.1:n.2185+16450G>A
ENST00000683270.1:c.6445+87G>A ENSP00000507624.1:n.6445+87G>A
ENST00000683367.1:c.2177-7851G>A ENSP00000507780.1:n.2177-7851G>A
ENST00000683489.1:c.2291+4250G>A ENSP00000508403.1:n.2291+4250G>A
ENST00000683680.1:c.2318+4250G>A ENSP00000507223.1:n.2318+4250G>A
ENST00000684163.1:c.2204-7851G>A ENSP00000508262.1:n.2204-7851G>A
ENST00000684196.1:n.4543-7851G>A
ENST00000684325.1:c.2186-15661G>A ENSP00000508121.1:n.2186-15661G>A
ENST00000684385.1:c.2221-7851G>A ENSP00000507855.1:n.2221-7851G>A
ENST00000684497.1:c.2186-14691G>A ENSP00000507057.1:n.2186-14691G>A
ENST00000382292.9:c.6541G>A MANE Select ENSP00000371729.3:p.Ala2181Thr
ENST00000423156.2:c.2186-7851G>A ENSP00000390925.2:n.2186-7851G>A
ENST00000455470.6:c.2431+4110G>A ENSP00000406565.2:n.2431+4110G>A
ENST00000382292.7:c.6541G>A ENSP00000371729.3:p.Ala2181Thr
ENST00000382298.7:c.6541G>A ENSP00000371735.3:p.Ala2181Thr
ENST00000402364.1:c.4291G>A ENSP00000385844.1:p.Ala1431Thr
ENST00000423156.1:c.1058-7851G>A ENSP00000390925.1:n.1058-7851G>A
ENST00000455470.5:c.2129+4110G>A
NM_001278055.1:c.6100G>A NP_001264984.1:p.Ala2034Thr
NM_014363.5:c.6541G>A NP_055178.3:p.Ala2181Thr
XM_005266338.1:c.6568G>A XP_005266395.1:p.Ala2190Thr
XM_011535038.1:c.6592G>A XP_011533340.1:p.Ala2198Thr
XM_011535039.1:c.6559G>A XP_011533341.1:p.Ala2187Thr
XM_005266338.2:c.6568G>A XP_005266395.1:p.Ala2190Thr
XM_011535039.2:c.6559G>A XP_011533341.1:p.Ala2187Thr
XM_017020539.1:c.6532G>A XP_016876028.1:p.Ala2178Thr
XM_024449337.1:c.6568G>A XP_024305105.1:p.Ala2190Thr
NM_014363.6:c.6541G>A MANE Select NP_055178.3:p.Ala2181Thr
NM_001278055.2:c.6100G>A NP_001264984.1:p.Ala2034Thr