Canonical Allele Identifier: CA387521500
Gene: SACS HGNC NCBI

Linked Data

dbSNP Id: rs2137608845

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23337337G>A , CM000675.2:g.23337337G>A GRCh38
NC_000013.10:g.23911476G>A , CM000675.1:g.23911476G>A GRCh37
NC_000013.9:g.22809476G>A NCBI36
NG_012342.1:g.101366C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2185+16448C>T ENSP00000508399.1:n.2185+16448C>T
ENST00000682944.1:c.6566C>T ENSP00000507173.1:p.Ala2189Val
ENST00000683210.1:c.2185+16448C>T ENSP00000506739.1:n.2185+16448C>T
ENST00000683270.1:c.6445+85C>T ENSP00000507624.1:n.6445+85C>T
ENST00000683367.1:c.2177-7853C>T ENSP00000507780.1:n.2177-7853C>T
ENST00000683489.1:c.2291+4248C>T ENSP00000508403.1:n.2291+4248C>T
ENST00000683680.1:c.2318+4248C>T ENSP00000507223.1:n.2318+4248C>T
ENST00000684163.1:c.2204-7853C>T ENSP00000508262.1:n.2204-7853C>T
ENST00000684196.1:n.4543-7853C>T
ENST00000684325.1:c.2186-15663C>T ENSP00000508121.1:n.2186-15663C>T
ENST00000684385.1:c.2221-7853C>T ENSP00000507855.1:n.2221-7853C>T
ENST00000684497.1:c.2186-14693C>T ENSP00000507057.1:n.2186-14693C>T
ENST00000382292.9:c.6539C>T MANE Select ENSP00000371729.3:p.Ala2180Val
ENST00000423156.2:c.2186-7853C>T ENSP00000390925.2:n.2186-7853C>T
ENST00000455470.6:c.2431+4108C>T ENSP00000406565.2:n.2431+4108C>T
ENST00000382292.7:c.6539C>T ENSP00000371729.3:p.Ala2180Val
ENST00000382298.7:c.6539C>T ENSP00000371735.3:p.Ala2180Val
ENST00000402364.1:c.4289C>T ENSP00000385844.1:p.Ala1430Val
ENST00000423156.1:c.1058-7853C>T ENSP00000390925.1:n.1058-7853C>T
ENST00000455470.5:c.2129+4108C>T
NM_001278055.1:c.6098C>T NP_001264984.1:p.Ala2033Val
NM_014363.5:c.6539C>T NP_055178.3:p.Ala2180Val
XM_005266338.1:c.6566C>T XP_005266395.1:p.Ala2189Val
XM_011535038.1:c.6590C>T XP_011533340.1:p.Ala2197Val
XM_011535039.1:c.6557C>T XP_011533341.1:p.Ala2186Val
XM_005266338.2:c.6566C>T XP_005266395.1:p.Ala2189Val
XM_011535039.2:c.6557C>T XP_011533341.1:p.Ala2186Val
XM_017020539.1:c.6530C>T XP_016876028.1:p.Ala2177Val
XM_024449337.1:c.6566C>T XP_024305105.1:p.Ala2189Val
NM_014363.6:c.6539C>T MANE Select NP_055178.3:p.Ala2180Val
NM_001278055.2:c.6098C>T NP_001264984.1:p.Ala2033Val