Canonical Allele Identifier: CA387536890
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 623396
dbSNP Id: rs1566071225

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23340821T>C , CM000675.2:g.23340821T>C GRCh38
NC_000013.10:g.23914960T>C , CM000675.1:g.23914960T>C GRCh37
NC_000013.9:g.22812960T>C NCBI36
NG_012342.1:g.97882A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2185+12964A>G ENSP00000508399.1:n.2185+12964A>G
ENST00000682944.1:c.3082A>G ENSP00000507173.1:p.Asn1028Asp
ENST00000683210.1:c.2185+12964A>G ENSP00000506739.1:n.2185+12964A>G
ENST00000683270.1:c.3046A>G ENSP00000507624.1:p.Asn1016Asp
ENST00000683367.1:c.2177-11337A>G ENSP00000507780.1:n.2177-11337A>G
ENST00000683489.1:c.2291+764A>G ENSP00000508403.1:n.2291+764A>G
ENST00000683680.1:c.2318+764A>G ENSP00000507223.1:n.2318+764A>G
ENST00000684163.1:c.2203+5990A>G ENSP00000508262.1:n.2203+5990A>G
ENST00000684196.1:n.4543-11337A>G
ENST00000684325.1:c.2185+12964A>G ENSP00000508121.1:n.2185+12964A>G
ENST00000684385.1:c.2220+5990A>G ENSP00000507855.1:n.2220+5990A>G
ENST00000684497.1:c.2185+12964A>G ENSP00000507057.1:n.2185+12964A>G
ENST00000382292.9:c.3055A>G MANE Select ENSP00000371729.3:p.Asn1019Asp
ENST00000423156.2:c.2186-11337A>G ENSP00000390925.2:n.2186-11337A>G
ENST00000455470.6:c.2431+624A>G ENSP00000406565.2:n.2431+624A>G
ENST00000382292.7:c.3055A>G ENSP00000371729.3:p.Asn1019Asp
ENST00000382298.7:c.3055A>G ENSP00000371735.3:p.Asn1019Asp
ENST00000402364.1:c.805A>G ENSP00000385844.1:p.Asn269Asp
ENST00000423156.1:c.1058-11337A>G ENSP00000390925.1:n.1058-11337A>G
ENST00000455470.5:c.2129+624A>G
NM_001278055.1:c.2614A>G NP_001264984.1:p.Asn872Asp
NM_014363.5:c.3055A>G NP_055178.3:p.Asn1019Asp
XM_005266338.1:c.3082A>G XP_005266395.1:p.Asn1028Asp
XM_011535038.1:c.3106A>G XP_011533340.1:p.Asn1036Asp
XM_011535039.1:c.3073A>G XP_011533341.1:p.Asn1025Asp
XM_005266338.2:c.3082A>G XP_005266395.1:p.Asn1028Asp
XM_011535039.2:c.3073A>G XP_011533341.1:p.Asn1025Asp
XM_017020539.1:c.3046A>G XP_016876028.1:p.Asn1016Asp
XM_024449337.1:c.3082A>G XP_024305105.1:p.Asn1028Asp
NM_014363.6:c.3055A>G MANE Select NP_055178.3:p.Asn1019Asp
NM_001278055.2:c.2614A>G NP_001264984.1:p.Asn872Asp