Canonical Allele Identifier: CA916083345

Gene: SACS

Linked Data

• ClinVar Variation Id: 841237
• ClinVar RCV Id: RCV001043420
• dbSNP Id: rs1868403104

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23334628del , CM000675.2:g.23334628del	GRCh38
NC_000013.10:g.23908767del , CM000675.1:g.23908767del	GRCh37
NC_000013.9:g.22806767del	NCBI36
NG_012342.1:g.104076del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+19158del	ENSP00000508399.1:n.2185+19158del
ENST00000682944.1:c.9276del	ENSP00000507173.1:p.Ile3093Ter
ENST00000683210.1:c.2185+19158del	ENSP00000506739.1:n.2185+19158del
ENST00000683270.1:c.6445+2795del	ENSP00000507624.1:n.6445+2795del
ENST00000683367.1:c.2177-5143del	ENSP00000507780.1:n.2177-5143del
ENST00000683489.1:c.2292-4675del	ENSP00000508403.1:n.2292-4675del
ENST00000683680.1:c.2319-4675del	ENSP00000507223.1:n.2319-4675del
ENST00000684163.1:c.2204-5143del	ENSP00000508262.1:n.2204-5143del
ENST00000684196.1:n.4543-5143del
ENST00000684325.1:c.2186-12953del	ENSP00000508121.1:n.2186-12953del
ENST00000684385.1:c.2221-5143del	ENSP00000507855.1:n.2221-5143del
ENST00000684497.1:c.2186-11983del	ENSP00000507057.1:n.2186-11983del
ENST00000382292.9:c.9249del MANE Select	ENSP00000371729.3:p.Ile3084Ter
ENST00000423156.2:c.2186-5143del	ENSP00000390925.2:n.2186-5143del
ENST00000455470.6:c.2432-5143del	ENSP00000406565.2:n.2432-5143del
ENST00000382292.7:c.9249del	ENSP00000371729.3:p.Ile3084Ter
ENST00000382298.7:c.9249del	ENSP00000371735.3:p.Ile3084Ter
ENST00000402364.1:c.6999del	ENSP00000385844.1:p.Ile2334Ter
ENST00000423156.1:c.1058-5143del	ENSP00000390925.1:n.1058-5143del
ENST00000455470.5:c.2130-5143del
NM_001278055.1:c.8808del	NP_001264984.1:p.Ile2937Ter
NM_014363.5:c.9249del	NP_055178.3:p.Ile3084Ter
XM_005266338.1:c.9276del	XP_005266395.1:p.Ile3093Ter
XM_011535038.1:c.9300del	XP_011533340.1:p.Ile3101Ter
XM_011535039.1:c.9267del	XP_011533341.1:p.Ile3090Ter
XM_005266338.2:c.9276del	XP_005266395.1:p.Ile3093Ter
XM_011535039.2:c.9267del	XP_011533341.1:p.Ile3090Ter
XM_017020539.1:c.9240del	XP_016876028.1:p.Ile3081Ter
XM_024449337.1:c.9276del	XP_024305105.1:p.Ile3093Ter
NM_014363.6:c.9249del MANE Select	NP_055178.3:p.Ile3084Ter
NM_001278055.2:c.8808del	NP_001264984.1:p.Ile2937Ter