Canonical Allele Identifier: CA387518870
Gene: SACS HGNC NCBI

Linked Data

dbSNP Id: rs1342628164

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23336362G>T , CM000675.2:g.23336362G>T GRCh38
NC_000013.10:g.23910501G>T , CM000675.1:g.23910501G>T GRCh37
NC_000013.9:g.22808501G>T NCBI36
NG_012342.1:g.102341C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2185+17423C>A ENSP00000508399.1:n.2185+17423C>A
ENST00000682944.1:c.7541C>A ENSP00000507173.1:p.Ala2514Asp
ENST00000683210.1:c.2185+17423C>A ENSP00000506739.1:n.2185+17423C>A
ENST00000683270.1:c.6445+1060C>A ENSP00000507624.1:n.6445+1060C>A
ENST00000683367.1:c.2177-6878C>A ENSP00000507780.1:n.2177-6878C>A
ENST00000683489.1:c.2291+5223C>A ENSP00000508403.1:n.2291+5223C>A
ENST00000683680.1:c.2318+5223C>A ENSP00000507223.1:n.2318+5223C>A
ENST00000684163.1:c.2204-6878C>A ENSP00000508262.1:n.2204-6878C>A
ENST00000684196.1:n.4543-6878C>A
ENST00000684325.1:c.2186-14688C>A ENSP00000508121.1:n.2186-14688C>A
ENST00000684385.1:c.2221-6878C>A ENSP00000507855.1:n.2221-6878C>A
ENST00000684497.1:c.2186-13718C>A ENSP00000507057.1:n.2186-13718C>A
ENST00000382292.9:c.7514C>A MANE Select ENSP00000371729.3:p.Ala2505Asp
ENST00000423156.2:c.2186-6878C>A ENSP00000390925.2:n.2186-6878C>A
ENST00000455470.6:c.2431+5083C>A ENSP00000406565.2:n.2431+5083C>A
ENST00000382292.7:c.7514C>A ENSP00000371729.3:p.Ala2505Asp
ENST00000382298.7:c.7514C>A ENSP00000371735.3:p.Ala2505Asp
ENST00000402364.1:c.5264C>A ENSP00000385844.1:p.Ala1755Asp
ENST00000423156.1:c.1058-6878C>A ENSP00000390925.1:n.1058-6878C>A
ENST00000455470.5:c.2129+5083C>A
NM_001278055.1:c.7073C>A NP_001264984.1:p.Ala2358Asp
NM_014363.5:c.7514C>A NP_055178.3:p.Ala2505Asp
XM_005266338.1:c.7541C>A XP_005266395.1:p.Ala2514Asp
XM_011535038.1:c.7565C>A XP_011533340.1:p.Ala2522Asp
XM_011535039.1:c.7532C>A XP_011533341.1:p.Ala2511Asp
XM_005266338.2:c.7541C>A XP_005266395.1:p.Ala2514Asp
XM_011535039.2:c.7532C>A XP_011533341.1:p.Ala2511Asp
XM_017020539.1:c.7505C>A XP_016876028.1:p.Ala2502Asp
XM_024449337.1:c.7541C>A XP_024305105.1:p.Ala2514Asp
NM_014363.6:c.7514C>A MANE Select NP_055178.3:p.Ala2505Asp
NM_001278055.2:c.7073C>A NP_001264984.1:p.Ala2358Asp