Canonical Allele Identifier: CA387536746

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23914896A>G (hg19) ; chr13:g.23340757A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23340757A>G , CM000675.2:g.23340757A>G	GRCh38
NC_000013.10:g.23914896A>G , CM000675.1:g.23914896A>G	GRCh37
NC_000013.9:g.22812896A>G	NCBI36
NG_012342.1:g.97946T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+13028T>C	ENSP00000508399.1:n.2185+13028T>C
ENST00000682944.1:c.3146T>C	ENSP00000507173.1:p.Ile1049Thr
ENST00000683210.1:c.2185+13028T>C	ENSP00000506739.1:n.2185+13028T>C
ENST00000683270.1:c.3110T>C	ENSP00000507624.1:p.Ile1037Thr
ENST00000683367.1:c.2177-11273T>C	ENSP00000507780.1:n.2177-11273T>C
ENST00000683489.1:c.2291+828T>C	ENSP00000508403.1:n.2291+828T>C
ENST00000683680.1:c.2318+828T>C	ENSP00000507223.1:n.2318+828T>C
ENST00000684163.1:c.2203+6054T>C	ENSP00000508262.1:n.2203+6054T>C
ENST00000684196.1:n.4543-11273T>C
ENST00000684325.1:c.2185+13028T>C	ENSP00000508121.1:n.2185+13028T>C
ENST00000684385.1:c.2220+6054T>C	ENSP00000507855.1:n.2220+6054T>C
ENST00000684497.1:c.2185+13028T>C	ENSP00000507057.1:n.2185+13028T>C
ENST00000382292.9:c.3119T>C MANE Select	ENSP00000371729.3:p.Ile1040Thr
ENST00000423156.2:c.2186-11273T>C	ENSP00000390925.2:n.2186-11273T>C
ENST00000455470.6:c.2431+688T>C	ENSP00000406565.2:n.2431+688T>C
ENST00000382292.7:c.3119T>C	ENSP00000371729.3:p.Ile1040Thr
ENST00000382298.7:c.3119T>C	ENSP00000371735.3:p.Ile1040Thr
ENST00000402364.1:c.869T>C	ENSP00000385844.1:p.Ile290Thr
ENST00000423156.1:c.1058-11273T>C	ENSP00000390925.1:n.1058-11273T>C
ENST00000455470.5:c.2129+688T>C
NM_001278055.1:c.2678T>C	NP_001264984.1:p.Ile893Thr
NM_014363.5:c.3119T>C	NP_055178.3:p.Ile1040Thr
XM_005266338.1:c.3146T>C	XP_005266395.1:p.Ile1049Thr
XM_011535038.1:c.3170T>C	XP_011533340.1:p.Ile1057Thr
XM_011535039.1:c.3137T>C	XP_011533341.1:p.Ile1046Thr
XM_005266338.2:c.3146T>C	XP_005266395.1:p.Ile1049Thr
XM_011535039.2:c.3137T>C	XP_011533341.1:p.Ile1046Thr
XM_017020539.1:c.3110T>C	XP_016876028.1:p.Ile1037Thr
XM_024449337.1:c.3146T>C	XP_024305105.1:p.Ile1049Thr
NM_014363.6:c.3119T>C MANE Select	NP_055178.3:p.Ile1040Thr
NM_001278055.2:c.2678T>C	NP_001264984.1:p.Ile893Thr