Canonical Allele Identifier: CA2622329306

Gene: SACS

Linked Data

• gnomAD v4: 13-23339122-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23339123del , CM000675.2:g.23339123del	GRCh38
NC_000013.10:g.23913262del , CM000675.1:g.23913262del	GRCh37
NC_000013.9:g.22811262del	NCBI36
NG_012342.1:g.99580del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+14662del	ENSP00000508399.1:n.2185+14662del
ENST00000682944.1:c.4780del	ENSP00000507173.1:p.Ile1594Ter
ENST00000683210.1:c.2185+14662del	ENSP00000506739.1:n.2185+14662del
ENST00000683270.1:c.4744del	ENSP00000507624.1:p.Ile1582Ter
ENST00000683367.1:c.2177-9639del	ENSP00000507780.1:n.2177-9639del
ENST00000683489.1:c.2291+2462del	ENSP00000508403.1:n.2291+2462del
ENST00000683680.1:c.2318+2462del	ENSP00000507223.1:n.2318+2462del
ENST00000684163.1:c.2203+7688del	ENSP00000508262.1:n.2203+7688del
ENST00000684196.1:n.4543-9639del
ENST00000684325.1:c.2185+14662del	ENSP00000508121.1:n.2185+14662del
ENST00000684385.1:c.2220+7688del	ENSP00000507855.1:n.2220+7688del
ENST00000684497.1:c.2185+14662del	ENSP00000507057.1:n.2185+14662del
ENST00000382292.9:c.4753del MANE Select	ENSP00000371729.3:p.Ile1585Ter
ENST00000423156.2:c.2186-9639del	ENSP00000390925.2:n.2186-9639del
ENST00000455470.6:c.2431+2322del	ENSP00000406565.2:n.2431+2322del
ENST00000382292.7:c.4753del	ENSP00000371729.3:p.Ile1585Ter
ENST00000382298.7:c.4753del	ENSP00000371735.3:p.Ile1585Ter
ENST00000402364.1:c.2503del	ENSP00000385844.1:p.Ile835Ter
ENST00000423156.1:c.1058-9639del	ENSP00000390925.1:n.1058-9639del
ENST00000455470.5:c.2129+2322del
NM_001278055.1:c.4312del	NP_001264984.1:p.Ile1438Ter
NM_014363.5:c.4753del	NP_055178.3:p.Ile1585Ter
XM_005266338.1:c.4780del	XP_005266395.1:p.Ile1594Ter
XM_011535038.1:c.4804del	XP_011533340.1:p.Ile1602Ter
XM_011535039.1:c.4771del	XP_011533341.1:p.Ile1591Ter
XM_005266338.2:c.4780del	XP_005266395.1:p.Ile1594Ter
XM_011535039.2:c.4771del	XP_011533341.1:p.Ile1591Ter
XM_017020539.1:c.4744del	XP_016876028.1:p.Ile1582Ter
XM_024449337.1:c.4780del	XP_024305105.1:p.Ile1594Ter
NM_014363.6:c.4753del MANE Select	NP_055178.3:p.Ile1585Ter
NM_001278055.2:c.4312del	NP_001264984.1:p.Ile1438Ter