Canonical Allele Identifier: CA483161362

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23911148T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23337009T>C , CM000675.2:g.23337009T>C	GRCh38
NC_000013.10:g.23911148T>C , CM000675.1:g.23911148T>C	GRCh37
NC_000013.9:g.22809148T>C	NCBI36
NG_012342.1:g.101694A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+16776A>G	ENSP00000508399.1:n.2185+16776A>G
ENST00000682944.1:c.6894A>G	ENSP00000507173.1:p.Thr2298=
ENST00000683210.1:c.2185+16776A>G	ENSP00000506739.1:n.2185+16776A>G
ENST00000683270.1:c.6445+413A>G	ENSP00000507624.1:n.6445+413A>G
ENST00000683367.1:c.2177-7525A>G	ENSP00000507780.1:n.2177-7525A>G
ENST00000683489.1:c.2291+4576A>G	ENSP00000508403.1:n.2291+4576A>G
ENST00000683680.1:c.2318+4576A>G	ENSP00000507223.1:n.2318+4576A>G
ENST00000684163.1:c.2204-7525A>G	ENSP00000508262.1:n.2204-7525A>G
ENST00000684196.1:n.4543-7525A>G
ENST00000684325.1:c.2186-15335A>G	ENSP00000508121.1:n.2186-15335A>G
ENST00000684385.1:c.2221-7525A>G	ENSP00000507855.1:n.2221-7525A>G
ENST00000684497.1:c.2186-14365A>G	ENSP00000507057.1:n.2186-14365A>G
ENST00000382292.9:c.6867A>G MANE Select	ENSP00000371729.3:p.Thr2289=
ENST00000423156.2:c.2186-7525A>G	ENSP00000390925.2:n.2186-7525A>G
ENST00000455470.6:c.2431+4436A>G	ENSP00000406565.2:n.2431+4436A>G
ENST00000382292.7:c.6867A>G	ENSP00000371729.3:p.Thr2289=
ENST00000382298.7:c.6867A>G	ENSP00000371735.3:p.Thr2289=
ENST00000402364.1:c.4617A>G	ENSP00000385844.1:p.Thr1539=
ENST00000423156.1:c.1058-7525A>G	ENSP00000390925.1:n.1058-7525A>G
ENST00000455470.5:c.2129+4436A>G
NM_001278055.1:c.6426A>G	NP_001264984.1:p.Thr2142=
NM_014363.5:c.6867A>G	NP_055178.3:p.Thr2289=
XM_005266338.1:c.6894A>G	XP_005266395.1:p.Thr2298=
XM_011535038.1:c.6918A>G	XP_011533340.1:p.Thr2306=
XM_011535039.1:c.6885A>G	XP_011533341.1:p.Thr2295=
XM_005266338.2:c.6894A>G	XP_005266395.1:p.Thr2298=
XM_011535039.2:c.6885A>G	XP_011533341.1:p.Thr2295=
XM_017020539.1:c.6858A>G	XP_016876028.1:p.Thr2286=
XM_024449337.1:c.6894A>G	XP_024305105.1:p.Thr2298=
NM_014363.6:c.6867A>G MANE Select	NP_055178.3:p.Thr2289=
NM_001278055.2:c.6426A>G	NP_001264984.1:p.Thr2142=