Canonical Allele Identifier: CA387506402

Gene: SACS

Linked Data

• COSMIC: COSM4046484 ; COSM4046485
• MyVariant Identifiers: chr13:g.23905080G>T (hg19) ; chr13:g.23330941G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23330941G>T , CM000675.2:g.23330941G>T	GRCh38
NC_000013.10:g.23905080G>T , CM000675.1:g.23905080G>T	GRCh37
NC_000013.9:g.22803080G>T	NCBI36
NG_012342.1:g.107762C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-18826C>A	ENSP00000508399.1:n.2186-18826C>A
ENST00000682944.1:c.12962C>A	ENSP00000507173.1:p.Ser4321Tyr
ENST00000683210.1:c.2185+22844C>A	ENSP00000506739.1:n.2185+22844C>A
ENST00000683270.1:c.6446-1457C>A	ENSP00000507624.1:n.6446-1457C>A
ENST00000683367.1:c.2177-1457C>A	ENSP00000507780.1:n.2177-1457C>A
ENST00000683489.1:c.2292-989C>A	ENSP00000508403.1:n.2292-989C>A
ENST00000683680.1:c.2319-989C>A	ENSP00000507223.1:n.2319-989C>A
ENST00000684163.1:c.2204-1457C>A	ENSP00000508262.1:n.2204-1457C>A
ENST00000684196.1:n.4543-1457C>A
ENST00000684325.1:c.2186-9267C>A	ENSP00000508121.1:n.2186-9267C>A
ENST00000684385.1:c.2221-1457C>A	ENSP00000507855.1:n.2221-1457C>A
ENST00000684497.1:c.2186-8297C>A	ENSP00000507057.1:n.2186-8297C>A
ENST00000382292.9:c.12935C>A MANE Select	ENSP00000371729.3:p.Ser4312Tyr
ENST00000423156.2:c.2186-1457C>A	ENSP00000390925.2:n.2186-1457C>A
ENST00000455470.6:c.2432-1457C>A	ENSP00000406565.2:n.2432-1457C>A
ENST00000382292.7:c.12935C>A	ENSP00000371729.3:p.Ser4312Tyr
ENST00000382298.7:c.12935C>A	ENSP00000371735.3:p.Ser4312Tyr
ENST00000402364.1:c.10685C>A	ENSP00000385844.1:p.Ser3562Tyr
ENST00000423156.1:c.1058-1457C>A	ENSP00000390925.1:n.1058-1457C>A
ENST00000455470.5:c.2130-1457C>A
NM_001278055.1:c.12494C>A	NP_001264984.1:p.Ser4165Tyr
NM_014363.5:c.12935C>A	NP_055178.3:p.Ser4312Tyr
XM_005266338.1:c.12962C>A	XP_005266395.1:p.Ser4321Tyr
XM_011535038.1:c.12986C>A	XP_011533340.1:p.Ser4329Tyr
XM_011535039.1:c.12953C>A	XP_011533341.1:p.Ser4318Tyr
XM_005266338.2:c.12962C>A	XP_005266395.1:p.Ser4321Tyr
XM_011535039.2:c.12953C>A	XP_011533341.1:p.Ser4318Tyr
XM_017020539.1:c.12926C>A	XP_016876028.1:p.Ser4309Tyr
XM_024449337.1:c.12962C>A	XP_024305105.1:p.Ser4321Tyr
NM_014363.6:c.12935C>A MANE Select	NP_055178.3:p.Ser4312Tyr
NM_001278055.2:c.12494C>A	NP_001264984.1:p.Ser4165Tyr