Canonical Allele Identifier: CA6911866
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2428011
ClinVar RCV Id: RCV003116982
dbSNP Id: rs748391057

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23354910C>T , CM000675.2:g.23354910C>T GRCh38
NC_000013.10:g.23929049C>T , CM000675.1:g.23929049C>T GRCh37
NC_000013.9:g.22827049C>T NCBI36
NG_012342.1:g.83793G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.1702G>A ENSP00000508399.1:p.Asp568Asn
ENST00000682944.1:c.1702G>A ENSP00000507173.1:p.Asp568Asn
ENST00000683154.1:n.1840G>A
ENST00000683210.1:c.1702G>A ENSP00000506739.1:p.Asp568Asn
ENST00000683270.1:c.1693G>A ENSP00000507624.1:p.Asp565Asn
ENST00000683367.1:c.1693G>A ENSP00000507780.1:p.Asp565Asn
ENST00000683489.1:c.1702G>A ENSP00000508403.1:p.Asp568Asn
ENST00000683680.1:c.1702G>A ENSP00000507223.1:p.Asp568Asn
ENST00000684163.1:c.1693G>A ENSP00000508262.1:p.Asp565Asn
ENST00000684196.1:n.4059G>A
ENST00000684325.1:c.1702G>A ENSP00000508121.1:p.Asp568Asn
ENST00000684385.1:c.1702G>A ENSP00000507855.1:p.Asp568Asn
ENST00000684497.1:c.1702G>A ENSP00000507057.1:p.Asp568Asn
ENST00000382292.9:c.1702G>A MANE Select ENSP00000371729.3:p.Asp568Asn
ENST00000423156.2:c.1702G>A ENSP00000390925.2:p.Asp568Asn
ENST00000455470.6:c.1702G>A ENSP00000406565.2:p.Asp568Asn
ENST00000382292.7:c.1702G>A ENSP00000371729.3:p.Asp568Asn
ENST00000382298.7:c.1702G>A ENSP00000371735.3:p.Asp568Asn
ENST00000402364.1:c.-549G>A ENSP00000385844.1:n.-549G>A
ENST00000423156.1:c.574G>A ENSP00000390925.1:p.Asp192Asn
ENST00000455470.5:c.1400G>A
NM_001278055.1:c.1261G>A NP_001264984.1:p.Asp421Asn
NM_014363.5:c.1702G>A NP_055178.3:p.Asp568Asn
XM_005266338.1:c.1702G>A XP_005266395.1:p.Asp568Asn
XM_011535038.1:c.1726G>A XP_011533340.1:p.Asp576Asn
XM_011535039.1:c.1693G>A XP_011533341.1:p.Asp565Asn
XM_005266338.2:c.1702G>A XP_005266395.1:p.Asp568Asn
XM_011535039.2:c.1693G>A XP_011533341.1:p.Asp565Asn
XM_017020539.1:c.1693G>A XP_016876028.1:p.Asp565Asn
XM_024449337.1:c.1702G>A XP_024305105.1:p.Asp568Asn
NM_014363.6:c.1702G>A MANE Select NP_055178.3:p.Asp568Asn
NM_001278055.2:c.1261G>A NP_001264984.1:p.Asp421Asn