Canonical Allele Identifier: CA483161160
Gene: SACS HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.23911472T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23337333T>G , CM000675.2:g.23337333T>G GRCh38
NC_000013.10:g.23911472T>G , CM000675.1:g.23911472T>G GRCh37
NC_000013.9:g.22809472T>G NCBI36
NG_012342.1:g.101370A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2185+16452A>C ENSP00000508399.1:n.2185+16452A>C
ENST00000682944.1:c.6570A>C ENSP00000507173.1:p.Ala2190=
ENST00000683210.1:c.2185+16452A>C ENSP00000506739.1:n.2185+16452A>C
ENST00000683270.1:c.6445+89A>C ENSP00000507624.1:n.6445+89A>C
ENST00000683367.1:c.2177-7849A>C ENSP00000507780.1:n.2177-7849A>C
ENST00000683489.1:c.2291+4252A>C ENSP00000508403.1:n.2291+4252A>C
ENST00000683680.1:c.2318+4252A>C ENSP00000507223.1:n.2318+4252A>C
ENST00000684163.1:c.2204-7849A>C ENSP00000508262.1:n.2204-7849A>C
ENST00000684196.1:n.4543-7849A>C
ENST00000684325.1:c.2186-15659A>C ENSP00000508121.1:n.2186-15659A>C
ENST00000684385.1:c.2221-7849A>C ENSP00000507855.1:n.2221-7849A>C
ENST00000684497.1:c.2186-14689A>C ENSP00000507057.1:n.2186-14689A>C
ENST00000382292.9:c.6543A>C MANE Select ENSP00000371729.3:p.Ala2181=
ENST00000423156.2:c.2186-7849A>C ENSP00000390925.2:n.2186-7849A>C
ENST00000455470.6:c.2431+4112A>C ENSP00000406565.2:n.2431+4112A>C
ENST00000382292.7:c.6543A>C ENSP00000371729.3:p.Ala2181=
ENST00000382298.7:c.6543A>C ENSP00000371735.3:p.Ala2181=
ENST00000402364.1:c.4293A>C ENSP00000385844.1:p.Ala1431=
ENST00000423156.1:c.1058-7849A>C ENSP00000390925.1:n.1058-7849A>C
ENST00000455470.5:c.2129+4112A>C
NM_001278055.1:c.6102A>C NP_001264984.1:p.Ala2034=
NM_014363.5:c.6543A>C NP_055178.3:p.Ala2181=
XM_005266338.1:c.6570A>C XP_005266395.1:p.Ala2190=
XM_011535038.1:c.6594A>C XP_011533340.1:p.Ala2198=
XM_011535039.1:c.6561A>C XP_011533341.1:p.Ala2187=
XM_005266338.2:c.6570A>C XP_005266395.1:p.Ala2190=
XM_011535039.2:c.6561A>C XP_011533341.1:p.Ala2187=
XM_017020539.1:c.6534A>C XP_016876028.1:p.Ala2178=
XM_024449337.1:c.6570A>C XP_024305105.1:p.Ala2190=
NM_014363.6:c.6543A>C MANE Select NP_055178.3:p.Ala2181=
NM_001278055.2:c.6102A>C NP_001264984.1:p.Ala2034=