Canonical Allele Identifier: CA483161477

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23911379T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23337240T>C , CM000675.2:g.23337240T>C	GRCh38
NC_000013.10:g.23911379T>C , CM000675.1:g.23911379T>C	GRCh37
NC_000013.9:g.22809379T>C	NCBI36
NG_012342.1:g.101463A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+16545A>G	ENSP00000508399.1:n.2185+16545A>G
ENST00000682944.1:c.6663A>G	ENSP00000507173.1:p.Thr2221=
ENST00000683210.1:c.2185+16545A>G	ENSP00000506739.1:n.2185+16545A>G
ENST00000683270.1:c.6445+182A>G	ENSP00000507624.1:n.6445+182A>G
ENST00000683367.1:c.2177-7756A>G	ENSP00000507780.1:n.2177-7756A>G
ENST00000683489.1:c.2291+4345A>G	ENSP00000508403.1:n.2291+4345A>G
ENST00000683680.1:c.2318+4345A>G	ENSP00000507223.1:n.2318+4345A>G
ENST00000684163.1:c.2204-7756A>G	ENSP00000508262.1:n.2204-7756A>G
ENST00000684196.1:n.4543-7756A>G
ENST00000684325.1:c.2186-15566A>G	ENSP00000508121.1:n.2186-15566A>G
ENST00000684385.1:c.2221-7756A>G	ENSP00000507855.1:n.2221-7756A>G
ENST00000684497.1:c.2186-14596A>G	ENSP00000507057.1:n.2186-14596A>G
ENST00000382292.9:c.6636A>G MANE Select	ENSP00000371729.3:p.Thr2212=
ENST00000423156.2:c.2186-7756A>G	ENSP00000390925.2:n.2186-7756A>G
ENST00000455470.6:c.2431+4205A>G	ENSP00000406565.2:n.2431+4205A>G
ENST00000382292.7:c.6636A>G	ENSP00000371729.3:p.Thr2212=
ENST00000382298.7:c.6636A>G	ENSP00000371735.3:p.Thr2212=
ENST00000402364.1:c.4386A>G	ENSP00000385844.1:p.Thr1462=
ENST00000423156.1:c.1058-7756A>G	ENSP00000390925.1:n.1058-7756A>G
ENST00000455470.5:c.2129+4205A>G
NM_001278055.1:c.6195A>G	NP_001264984.1:p.Thr2065=
NM_014363.5:c.6636A>G	NP_055178.3:p.Thr2212=
XM_005266338.1:c.6663A>G	XP_005266395.1:p.Thr2221=
XM_011535038.1:c.6687A>G	XP_011533340.1:p.Thr2229=
XM_011535039.1:c.6654A>G	XP_011533341.1:p.Thr2218=
XM_005266338.2:c.6663A>G	XP_005266395.1:p.Thr2221=
XM_011535039.2:c.6654A>G	XP_011533341.1:p.Thr2218=
XM_017020539.1:c.6627A>G	XP_016876028.1:p.Thr2209=
XM_024449337.1:c.6663A>G	XP_024305105.1:p.Thr2221=
NM_014363.6:c.6636A>G MANE Select	NP_055178.3:p.Thr2212=
NM_001278055.2:c.6195A>G	NP_001264984.1:p.Thr2065=