Canonical Allele Identifier: CA387506828

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23905183G>T (hg19) ; chr13:g.23331044G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23331044G>T , CM000675.2:g.23331044G>T	GRCh38
NC_000013.10:g.23905183G>T , CM000675.1:g.23905183G>T	GRCh37
NC_000013.9:g.22803183G>T	NCBI36
NG_012342.1:g.107659C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-18929C>A	ENSP00000508399.1:n.2186-18929C>A
ENST00000682944.1:c.12859C>A	ENSP00000507173.1:p.Pro4287Thr
ENST00000683210.1:c.2185+22741C>A	ENSP00000506739.1:n.2185+22741C>A
ENST00000683270.1:c.6446-1560C>A	ENSP00000507624.1:n.6446-1560C>A
ENST00000683367.1:c.2177-1560C>A	ENSP00000507780.1:n.2177-1560C>A
ENST00000683489.1:c.2292-1092C>A	ENSP00000508403.1:n.2292-1092C>A
ENST00000683680.1:c.2319-1092C>A	ENSP00000507223.1:n.2319-1092C>A
ENST00000684163.1:c.2204-1560C>A	ENSP00000508262.1:n.2204-1560C>A
ENST00000684196.1:n.4543-1560C>A
ENST00000684325.1:c.2186-9370C>A	ENSP00000508121.1:n.2186-9370C>A
ENST00000684385.1:c.2221-1560C>A	ENSP00000507855.1:n.2221-1560C>A
ENST00000684497.1:c.2186-8400C>A	ENSP00000507057.1:n.2186-8400C>A
ENST00000382292.9:c.12832C>A MANE Select	ENSP00000371729.3:p.Pro4278Thr
ENST00000423156.2:c.2186-1560C>A	ENSP00000390925.2:n.2186-1560C>A
ENST00000455470.6:c.2432-1560C>A	ENSP00000406565.2:n.2432-1560C>A
ENST00000382292.7:c.12832C>A	ENSP00000371729.3:p.Pro4278Thr
ENST00000382298.7:c.12832C>A	ENSP00000371735.3:p.Pro4278Thr
ENST00000402364.1:c.10582C>A	ENSP00000385844.1:p.Pro3528Thr
ENST00000423156.1:c.1058-1560C>A	ENSP00000390925.1:n.1058-1560C>A
ENST00000455470.5:c.2130-1560C>A
NM_001278055.1:c.12391C>A	NP_001264984.1:p.Pro4131Thr
NM_014363.5:c.12832C>A	NP_055178.3:p.Pro4278Thr
XM_005266338.1:c.12859C>A	XP_005266395.1:p.Pro4287Thr
XM_011535038.1:c.12883C>A	XP_011533340.1:p.Pro4295Thr
XM_011535039.1:c.12850C>A	XP_011533341.1:p.Pro4284Thr
XM_005266338.2:c.12859C>A	XP_005266395.1:p.Pro4287Thr
XM_011535039.2:c.12850C>A	XP_011533341.1:p.Pro4284Thr
XM_017020539.1:c.12823C>A	XP_016876028.1:p.Pro4275Thr
XM_024449337.1:c.12859C>A	XP_024305105.1:p.Pro4287Thr
NM_014363.6:c.12832C>A MANE Select	NP_055178.3:p.Pro4278Thr
NM_001278055.2:c.12391C>A	NP_001264984.1:p.Pro4131Thr