Canonical Allele Identifier: CA387520543

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23911134A>G (hg19) ; chr13:g.23336995A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23336995A>G , CM000675.2:g.23336995A>G	GRCh38
NC_000013.10:g.23911134A>G , CM000675.1:g.23911134A>G	GRCh37
NC_000013.9:g.22809134A>G	NCBI36
NG_012342.1:g.101708T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+16790T>C	ENSP00000508399.1:n.2185+16790T>C
ENST00000682944.1:c.6908T>C	ENSP00000507173.1:p.Ile2303Thr
ENST00000683210.1:c.2185+16790T>C	ENSP00000506739.1:n.2185+16790T>C
ENST00000683270.1:c.6445+427T>C	ENSP00000507624.1:n.6445+427T>C
ENST00000683367.1:c.2177-7511T>C	ENSP00000507780.1:n.2177-7511T>C
ENST00000683489.1:c.2291+4590T>C	ENSP00000508403.1:n.2291+4590T>C
ENST00000683680.1:c.2318+4590T>C	ENSP00000507223.1:n.2318+4590T>C
ENST00000684163.1:c.2204-7511T>C	ENSP00000508262.1:n.2204-7511T>C
ENST00000684196.1:n.4543-7511T>C
ENST00000684325.1:c.2186-15321T>C	ENSP00000508121.1:n.2186-15321T>C
ENST00000684385.1:c.2221-7511T>C	ENSP00000507855.1:n.2221-7511T>C
ENST00000684497.1:c.2186-14351T>C	ENSP00000507057.1:n.2186-14351T>C
ENST00000382292.9:c.6881T>C MANE Select	ENSP00000371729.3:p.Ile2294Thr
ENST00000423156.2:c.2186-7511T>C	ENSP00000390925.2:n.2186-7511T>C
ENST00000455470.6:c.2431+4450T>C	ENSP00000406565.2:n.2431+4450T>C
ENST00000382292.7:c.6881T>C	ENSP00000371729.3:p.Ile2294Thr
ENST00000382298.7:c.6881T>C	ENSP00000371735.3:p.Ile2294Thr
ENST00000402364.1:c.4631T>C	ENSP00000385844.1:p.Ile1544Thr
ENST00000423156.1:c.1058-7511T>C	ENSP00000390925.1:n.1058-7511T>C
ENST00000455470.5:c.2129+4450T>C
NM_001278055.1:c.6440T>C	NP_001264984.1:p.Ile2147Thr
NM_014363.5:c.6881T>C	NP_055178.3:p.Ile2294Thr
XM_005266338.1:c.6908T>C	XP_005266395.1:p.Ile2303Thr
XM_011535038.1:c.6932T>C	XP_011533340.1:p.Ile2311Thr
XM_011535039.1:c.6899T>C	XP_011533341.1:p.Ile2300Thr
XM_005266338.2:c.6908T>C	XP_005266395.1:p.Ile2303Thr
XM_011535039.2:c.6899T>C	XP_011533341.1:p.Ile2300Thr
XM_017020539.1:c.6872T>C	XP_016876028.1:p.Ile2291Thr
XM_024449337.1:c.6908T>C	XP_024305105.1:p.Ile2303Thr
NM_014363.6:c.6881T>C MANE Select	NP_055178.3:p.Ile2294Thr
NM_001278055.2:c.6440T>C	NP_001264984.1:p.Ile2147Thr